m-Anisoyl chloride → HCID 4183341, compound

HRID 2236082Notes

Reaction equation

HRID 2236082 reaction equation
[C:1]([N:4]1[CH2:9][CH2:8][C:7]2[C:10]([C:14]#[N:15])=[C:11]([NH2:13])[S:12][C:6]=2[CH2:5]1)(=[O:3])[CH3:2].[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH:24]=[CH:25][CH:26]=1)[C:21](Cl)=[O:22]>>[C:1]([N:4]1[CH2:9][CH2:8][C:7]2[C:10]([C:14]#[N:15])=[C:11]([NH:13][C:21](=[O:22])[C:20]3[CH:24]=[CH:25][CH:26]=[C:18]([O:17][CH3:16])[CH:19]=3)[S:12][C:6]=2[CH2:5]1)(=[O:3])[CH3:2]

Participants

3

Reactant 2

HCID 74374m-Anisoyl chlorideHCID 422816726-Acetyl-2-amino-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carbonitrile2×

Product 1

HCID 4183341HCID 4183341, compound

Procedure

Prepared according to general procedure A starting from 6-acetyl-2-amino-3-cyano4,5,6,7-tetrahydro-thieno[2,3-c]pyridine (compound A3) and 3-methoxybenzoyl chloride.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-9579beab05964aef9fdc10cb98753bf4
Source dataset
uspto-grants-2010_05
Patent number
US07714134B2

Reaction notes

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