4-Chloroindole → HCID 10295964, compound
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][NH:6]2.[CH:11]([C:13]1[O:17][C:16]([C:18]([OH:20])=[O:19])=[CH:15][CH:14]=1)=O>>[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4]([CH:11]([C:4]1[C:3]3[C:7](=[CH:8][CH:9]=[CH:10][C:2]=3[Cl:1])[NH:6][CH:5]=1)[C:13]1[O:17][C:16]([C:18]([OH:20])=[O:19])=[CH:15][CH:14]=1)=[CH:5][NH:6]2Participants
3
Procedure
The compound Bis(4-chloroindol-3-yl)-(5-carboxy-2-furyl)methane was prepared following procedure A, starting from 4-chloro indole and 5-formyl 2-furan carboxylic acid. LC: Tr 2.31 min, MS: 425 (M+H)+
Workup
- customTr 2.31 min, MS
Sources & evidence
- ORD record
- ord-a28cc5ba1f8a468dbed33a4cd9685f17
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07022730B2
Reaction notes
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