Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 885271-40-9 Chemical Structure| 885271-40-9

Structure of 885271-40-9

Chemical Structure| 885271-40-9

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 885271-40-9 ]

CAS No. :885271-40-9
Formula : C14H20N2O2
M.W : 248.32
SMILES Code : O=C(N1CC2=C(C=C(CN)C=C2)C1)OC(C)(C)C
English Name :tert-Butyl 5-(aminomethyl)-2,3-dihydro-1H-isoindole-2-carboxylate
MDL No. :MFCD08234857

Safety of [ 885271-40-9 ]

Application In Synthesis of [ 885271-40-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 885271-40-9 ]

[ 885271-40-9 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 2390404-89-2 ]
  • [ 885271-40-9 ]
  • [ 2649490-14-0 ]
YieldReaction ConditionsOperation in experiment
58% With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 0 - 20℃; for 2h; 8.3 General procedure: Step 6: To a solution of (4-bromo-1H-pyrrolo[2,3-c]pyridin-2-yl)methanamine hydrochloride (233 mg, 0.78 mmol) in DMF (10 mL, 0.08 mmol) was added ((2R,4R)-1-(tert-butoxycarbonyl)-4-phenylpyrrolidine-2-carbonyl)-L-alanine (217 mg, 0.6 mmol). The resulting mixture was cooled to 0° C. HBTU (296 mg, 0.78 mmol) and DIEA (0.42 mL, 2.4 mmol) were added to the above mixture. After stirring for 30 min at the same temperature, the reaction was warmed to room temperature. The reaction was stirred for 90 min then concentrated under vacuum. The residue was dissolved in ethyl acetate-CH2Cl2 then washed with 10% KHSO4, H2O, sat. aq NaHCO3, and brine. The organic layer was dried over anhydrous Na2SO4 and concentrated under vacuum. The residue was purified by chromatography (0-100% [5% 7 N NH3 in MeOH/CH2Cl2]-CH2Cl2) to give tert-butyl (2R,4R)-2-(((S)-1-(((4-bromo-1H-pyrrolo[2,3-c]pyridin-2-yl)methyl)amino)-1-oxopropan-2-yl)carbamoyl)-4-phenylpyrrolidine-1-carboxylate (22 mg, 5% yield).
  • 2
  • [ 885271-40-9 ]
  • [ 1595742-54-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: triethylamine / dichloromethane / 20 °C 2: hydrogenchloride / 1,4-dioxane / 20 °C
  • 3
  • [ 885271-40-9 ]
  • [ 2821787-79-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: triethylamine / dichloromethane / 20 °C 2: hydrogenchloride / 1,4-dioxane / 20 °C 3: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C
  • 4
  • [ 885271-40-9 ]
  • [ 2821787-40-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: triethylamine / dichloromethane / 20 °C 2: hydrogenchloride / 1,4-dioxane / 20 °C 3: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C 4: hydrogenchloride / 1,4-dioxane / 20 °C
  • 5
  • [ 885271-40-9 ]
  • [ 2821787-82-8 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: acetonitrile / 8 h / 20 °C 2: hydrogenchloride / 1,4-dioxane / 20 °C
  • 6
  • [ 885271-40-9 ]
  • [ 2821787-83-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: acetonitrile / 8 h / 20 °C 2: hydrogenchloride / 1,4-dioxane / 20 °C 3: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C
  • 7
  • [ 885271-40-9 ]
  • [ 2821787-41-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: acetonitrile / 8 h / 20 °C 2: hydrogenchloride / 1,4-dioxane / 20 °C 3: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C 4: hydrogenchloride / 1,4-dioxane / 20 °C
  • 8
  • [ 885271-40-9 ]
  • [ 2305948-69-8 ]
  • [ 2821787-80-6 ]
YieldReaction ConditionsOperation in experiment
76.7% In acetonitrile at 20℃; for 8h; 8 Example 8. N-({2-[(2R)-2-amino-3-(2,4-dichlorophenyl)propanoyl]-2,3-dihydro- lH-isoindol-5-yl}methyl)methanesulfonoimidamide tert-butyl 5-(methanesulfonoimidamidomethyl)-2,3-dihydro-lH-isoindole-2- carboxylate [00163] 1 -(N-(tert-butyldimethylsilyl)-S-methylsulfonimidoyl)-3-methyl-lH-imidazol-3- ium trifluoromethane-sulfonate (4.3 g, 10.1 mmol) was added to a solution of tert-butyl 5- (aminomethyl)-2,3-dihydro-lH-isoindole-2-carboxylate (2.3 g, 9.2 mmol) in CH3CN (20 mL). The reaction mixture was stirred at r.t. for 8 h, and then CLLCN was distilled off. The aqueous solution was extracted with dichloromethane (3 c 50 mL). The organic extract was dried over sodium sulfate and concentrated to obtain tert-butyl 5- (methanesulfonoimidamidomethyl)-2,3-dihydro-lH-isoindole-2-carboxylate (2.3 g, 76.7% yield).
76.7% In acetonitrile at 20℃; for 8h; 8 Example 8. N-({2-[(2R)-2-amino-3-(2,4-dichlorophenyl)propanoyl]-2,3-dihydro- lH-isoindol-5-yl}methyl)methanesulfonoimidamide tert-butyl 5-(methanesulfonoimidamidomethyl)-2,3-dihydro-lH-isoindole-2- carboxylate [00163] 1 -(N-(tert-butyldimethylsilyl)-S-methylsulfonimidoyl)-3-methyl-lH-imidazol-3- ium trifluoromethane-sulfonate (4.3 g, 10.1 mmol) was added to a solution of tert-butyl 5- (aminomethyl)-2,3-dihydro-lH-isoindole-2-carboxylate (2.3 g, 9.2 mmol) in CH3CN (20 mL). The reaction mixture was stirred at r.t. for 8 h, and then CLLCN was distilled off. The aqueous solution was extracted with dichloromethane (3 c 50 mL). The organic extract was dried over sodium sulfate and concentrated to obtain tert-butyl 5- (methanesulfonoimidamidomethyl)-2,3-dihydro-lH-isoindole-2-carboxylate (2.3 g, 76.7% yield).
 

Historical Records