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| 1179014-45-9 Chemical Structure| 1179014-45-9

Structure of 1179014-45-9

Chemical Structure| 1179014-45-9

*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 [ 1179014-45-9 ]

CAS No. :1179014-45-9
Formula : C10H14N2O2S
M.W : 226.30
SMILES Code : NC1=CC=CC2=C1CCN(S(=O)(C)=O)C2
English Name :2-Methanesulfonyl-1,2,3,4-tetrahydroisoquinolin-5-amine
MDL No. :MFCD12821604

Safety of [ 1179014-45-9 ]

Application In Synthesis of [ 1179014-45-9 ]

* 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 [ 1179014-45-9 ]

[ 1179014-45-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 52328-48-0 ]
  • [ 1179014-45-9 ]
  • [ 223698-54-2 ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 25℃; for 18h;
  • 2
  • [ 1515224-57-3 ]
  • [ 1179014-45-9 ]
  • [ 1628527-80-9 ]
YieldReaction ConditionsOperation in experiment
With chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2′,4′,6′-tri-1-propyl-1,1′-biphenyl][2-(2-aminoethyl)phenyl]palladium(II); potassium <i>tert</i>-butylate In tetrahydrofuran; <i>tert</i>-butyl alcohol at 100℃; for 72h; 261 Example 256 4-chloro-N-(4-chlorophenyl)-3-{6-methyl-1H-imidazo[4,5-b]pyridin-2-yl}aniline To a solution of bromide I-4 (15 mg, 0.046 mmol, 1 eq.) and 4-chloroaniline DIEA (, 0.116 mmol, 2.5 eq.) in degassed tert-butanol was added potassium tert-butoxide (solution 1M in THF) (184 ul, 0.184 mmol, 4 eq.), BINAP (2.8 mg, 0.004 mmol, 0.1 eq) and Pd2(dba)3 (2.1 mg, 0.002 mmol, 0.05 eq). The resultant mixture was heated at 100° C. for 72 hrs. The reaction was filtered and the residue purified by reverse phase HPLC to afford Example 256. The TFA salt was neutralized by passing a methanolic solution of the compound through a bicarbonate resin. Syntheses of Examples 258 to 261 Examples 258 to 261 were synthesized using a protocol analogous to the one described above using Chloro(2-dicyclohexylphosphino-2′,4′,6′-tri-1-propyl-1,1′-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II) as catalyst.
 

Historical Records

Categories