5-(3,5-Dichlorophenyl)furan-2-carboxylic acid → 5-(3,5-Dichloro-phenyl)-furan-2-carboxylic acid (3-cyanomethyl-phenyl)-amide
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2[O:13][C:12]([C:14]([OH:16])=O)=[CH:11][CH:10]=2)[CH:5]=[C:6]([Cl:8])[CH:7]=1.[NH2:17][C:18]1[CH:19]=[C:20]([CH2:24][C:25]#[N:26])[CH:21]=[CH:22][CH:23]=1>>[C:25]([CH2:24][C:20]1[CH:19]=[C:18]([NH:17][C:14]([C:12]2[O:13][C:9]([C:4]3[CH:5]=[C:6]([Cl:8])[CH:7]=[C:2]([Cl:1])[CH:3]=3)=[CH:10][CH:11]=2)=[O:16])[CH:23]=[CH:22][CH:21]=1)#[N:26]Participants
3
Procedure
Carboxylic acid (67) (62 mg, 0.24 mmol) was coupled to aniline (80) (32 mg, 0.24 mmol) using Method C. After work-up, the solid was recrystallised from MeCN (3 ml) to give the title compound.
Workup
- customAfter work-up, the solid was recrystallised from MeCN (3 ml)
Sources & evidence
- ORD record
- ord-0edc002a353245bdaa66fd3036b99c57
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07803841B2
Reaction notes
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