m-Anisoyl chloride → HCID 59301487, compound

HRID 2236076Notes

Reaction equation

HRID 2236076 reaction equation
[CH3:1][C:2]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11]2[C:14]([C:18]#[N:19])=[C:15]([NH2:17])[S:16][C:10]=2[CH2:9]1)=[O:7])([CH3:4])[CH3:3].[CH3:20][O:21][C:22]1[CH:23]=[C:24]([CH:28]=[CH:29][CH:30]=1)[C:25](Cl)=[O:26]>>[C:2]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11]2[C:14]([C:18]#[N:19])=[C:15]([NH:17][C:25](=[O:26])[C:24]3[CH:28]=[CH:29][CH:30]=[C:22]([O:21][CH3:20])[CH:23]=3)[S:16][C:10]=2[CH2:9]1)=[O:7])([CH3:1])([CH3:3])[CH3:4]

Participants

3

Reactant 2

HCID 74374m-Anisoyl chlorideHCID 2763861tert-butyl 2-amino-3-cyano-4,7-dihydrothieno[2,3-c]pyridine-6(5H)-carboxylate2×

Product 1

HCID 59301487HCID 59301487, compound

Procedure

Prepared according to general procedure A starting from 2-amino-3-cyano-4,7-dihydro-thieno[2,3-c]pyridine-6(5H)-carboxylic acid 1,1-dimethylethyl ester (compound A2) and 3-methoxybenzoyl chloride.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-d437ffdc9dfe436383951f577786b662
Source dataset
uspto-grants-2010_05
Patent number
US07714134B2

Reaction notes

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