Benzo(b)thiophene-2-carboxylic acid → N-(3-cyano-4-piperidinophenyl)benzo[b]thiophene-2-carboxamide
Reaction equation
[S:1]1[C:5]([C:6]([OH:8])=O)=[CH:4][C:3]2[CH:9]=[CH:10][CH:11]=[CH:12][C:2]1=2.[NH2:13][C:14]1[CH:15]=[CH:16][C:17]([N:22]2[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]2)=[C:18]([CH:21]=1)[C:19]#[N:20]>>[C:19]([C:18]1[CH:21]=[C:14]([NH:13][C:6]([C:5]2[S:1][C:2]3[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=3[CH:4]=2)=[O:8])[CH:15]=[CH:16][C:17]=1[N:22]1[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]1)#[N:20]Participants
3
Procedure
By the reaction and treatment in the same manner as in Example 6 using benzo[b]thiophene-2-carboxylic acid (1.7 g) and 5-amino-2-piperidinobenzonitrile (2.0 g), the title compound (1.0 g) was obtained. melting point: 219-245° C.
Sources & evidence
- ORD record
- ord-a000118ec2f64c37a47e7715ae865d8b
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07112594B2
Reaction notes
Loading…