Home Cart Sign in  
Chemical Structure| 229007-09-4 Chemical Structure| 229007-09-4

Structure of 229007-09-4

Chemical Structure| 229007-09-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

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

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

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

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

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

Alternative Products

Product Details of [ 229007-09-4 ]

CAS No. :229007-09-4
Formula : C13H20N2O
M.W : 220.31
SMILES Code : CN(CC1=CC=C(N)C=C1)C2CCOCC2

Safety of [ 229007-09-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 229007-09-4 ]

* 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 [ 229007-09-4 ]

[ 229007-09-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 27018-76-4 ]
  • [ 229007-09-4 ]
  • [ 874889-01-7 ]
YieldReaction ConditionsOperation in experiment
71% EDCI (0.33 mmol, 0.07 g) was added in one portion to a suspension of (4-amino-benzyl)-methyl-(tetrahydro-pyran-4-yl)-amine Compound Id (0.25 mmol, 0.06 g), 1-benzyl-lH-indole-3-carboxylic acid Compound 13a (0.22 mmol, 0.06 g) and HOBt (0.22 mmol, 0.03g) in DMF (5.0 mL) at 0C. The resulting suspension was warmed to r.t. and then a crystal ofDMAP and Et3N (0.65 mmol, 0.1 mL) was added and the reaction mixture was stirredovernight. The orange-yellow suspension was poured in'water and was extracted with EtOAc(25 mL). The organic layer was washed with water (2 X 20 mL) followed by 5% NaOHsolution (10 mL) and brine. The organic layer was separated, dried over Na2SO4 and filtered.The solvent was removed in vacua and the resulting residue was purified by preparative TLC(15:1 CH2Cl2/MeOH) to yield Compound 13b as a pale yellow solid (0.07 g, 71%). MS m/e454 (M*H, 100%).; lodomethane (0.5 mL) was added to a solution of Compound 13b (0.08 mmol, 0.04 g)in CH2C12 (1.0 mL) at r.t. The mixture was allowed to stand overnight and a yellow precipitatewas observed. The solvent was removed in vacua and the yellow solid was washed with Et2Oto obtain Compound 162 as a yellow solid (0.05 g, 84%). MS m/e 469 (M+H, 100%).
71% With dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 0 - 20℃; EDCI (0.33 mmol, 0.07 g) was added in one portion to a suspension of (4-amino-benzyl)-methyl-(tetrahydro-pyran -4-yl)-amine Compound 1d (0.25 mmol, 0.06 g), <strong>[27018-76-4]1-benzyl-1H-indole-3-carboxylic acid</strong> Compound 13a (0.22 mmol, 0.06 g) and HOBt (0.22 mmol, 0.03 g) in DMF (5.0 mL) at 0 C. The resulting suspension was warmed to r.t. and then a crystal of DMAP and Et3N (0.65 mmol, 0.1 mL) was added and the reaction mixture was stirred overnight. The orange-yellow suspension was poured in water and was extracted with EtOAc (25 mL). The organic layer was washed with water (2×20 mL) followed by 5% NaOH solution (10 mL) and brine. The organic layer was separated, dried over Na2SO4 and filtered. The solvent was removed in vacuo and the resulting residue was purified by preparative TLC (15:1 CH2Cl2/MeOH) to yield Compound 13b as a pale yellow solid (0.07 g, 71%). MS m/e 454 (M+H, 100%).
 

Historical Records

Technical Information

Categories