5-(4-Fluorophenyl)thiophene-2-carboxylic acid → 2-Cyano-N-[5-(4-(1,1-dimethylethyl)phenyl)thien-2-yl]-3-hydroxybut-2-enamide
Reaction equation
[C:1]([C:3](=[C:19]([OH:21])[CH3:20])[C:4]([NH:6][C:7]1[S:8][C:9]([C:12]2[CH:17]=[CH:16][C:15](F)=[CH:14][CH:13]=2)=[CH:10][CH:11]=1)=[O:5])#[N:2].C(C1S[C:27]([C:30]2[CH:35]=CC(F)=C[CH:31]=2)=CC=1)(O)=O>>[C:1]([C:3](=[C:19]([OH:21])[CH3:20])[C:4]([NH:6][C:7]1[S:8][C:9]([C:12]2[CH:17]=[CH:16][C:15]([C:30]([CH3:35])([CH3:31])[CH3:27])=[CH:14][CH:13]=2)=[CH:10][CH:11]=1)=[O:5])#[N:2]Participants
3
Procedure
2-Cyano-N-[5-(4-fluorophenyl)thien-2-yl]-3-hydroxybut-2-enamide, m.p. 232°-234° C. (from 2-carboxy-5-(4-fluorophenyl)thiophene).
Sources & evidence
- ORD record
- ord-3796423922af4b71abd4410acfc6a153
- Source dataset
- uspto-grants-1991_01
- Patent number
- US04983619
Reaction notes
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