Butyryl chloride → HCID 68636343, compound
Reaction equation
[C:1]([C:3]1[C:11]2[CH2:10][CH2:9][NH:8][CH2:7][C:6]=2[S:5][C:4]=1[NH:12][C:13](=[O:24])[C:14]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[C:16]([O:22][CH3:23])[CH:15]=1)#[N:2].[C:25](Cl)(=[O:29])[CH2:26][CH2:27]C>>[C:1]([C:3]1[C:11]2[CH2:10][CH2:9][NH:8][CH:7]([C:25]([CH2:26][CH3:27])=[O:29])[C:6]=2[S:5][C:4]=1[NH:12][C:13](=[O:24])[C:14]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[C:16]([O:22][CH3:23])[CH:15]=1)#[N:2]Participants
3
Procedure
Prepared according to general procedure A starting from N-(3-cyano-4,5,6,7-tetrahydro-thieno[2,3-c]pyridin-2-yl)-3,5-dimethoxybenzamide (compound B1) and butyric acid chloride.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-ac06900e1eeb409a91b665ece4c5dd23
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07714134B2
Reaction notes
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