Benzoyl chloride → HCID 4384412, compound
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].[C:16](Cl)(=[O:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[C:1]([N:4]1[CH2:9][CH2:8][C:7]2[C:10]([C:14]#[N:15])=[C:11]([NH:13][C:16](=[O:23])[C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[S:12][C:6]=2[CH2:5]1)(=[O:3])[CH3:2]Participants
3
Procedure
Prepared according to general procedure A starting from 6-acetyl-2-amino-3-cyano-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine (compound A3) and benzoyl chloride.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-a7c2a2c556c042d8b78a247d17e6b3a9
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07714134B2
Reaction notes
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