3,5-Dimethoxybenzoyl chloride → HCID 4572353, compound

HRID 2236080Notes

Reaction equation

HRID 2236080 reaction equation
[CH2:1]([O:3][C:4]([N:6]1[CH2:11][CH2:10][C:9]2[C:12]([C:16]#[N:17])=[C:13]([NH2:15])[S:14][C:8]=2[CH2:7]1)=[O:5])[CH3:2].[CH3:18][O:19][C:20]1[CH:21]=[C:22]([CH:26]=[C:27]([O:29][CH3:30])[CH:28]=1)[C:23](Cl)=[O:24]>>[CH2:1]([O:3][C:4]([N:6]1[CH2:11][CH2:10][C:9]2[C:12]([C:16]#[N:17])=[C:13]([NH:15][C:23](=[O:24])[C:22]3[CH:26]=[C:27]([O:29][CH3:30])[CH:28]=[C:20]([O:19][CH3:18])[CH:21]=3)[S:14][C:8]=2[CH2:7]1)=[O:5])[CH3:2]

Participants

3

Reactant 2

HCID 870033,5-Dimethoxybenzoyl chlorideHCID 2816609ethyl 2-amino-3-cyano-5,7-dihydro-4H-thieno[2,3-c]pyridine-6-carboxylate2×

Product 1

HCID 4572353HCID 4572353, 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 ethyl ester (compound A1) and 3,5-dimethoxy benzoyl chloride.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-f6c1910565234a78a6b5ceb1baad9840
Source dataset
uspto-grants-2010_05
Patent number
US07714134B2

Reaction notes

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