Cyclopropaneacetic acid → HCID 18368161, compound
Reaction equation
[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[NH:4][C:3]=1[C:12](=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[CH:20]1([CH2:23][C:24](O)=[O:25])[CH2:22][CH2:21]1>>[C:12]([C:3]1[NH:4][C:5]2[C:10]([C:2]=1[NH:1][C:24](=[O:25])[CH2:23][CH:20]1[CH2:22][CH2:21]1)=[CH:9][CH:8]=[C:7]([Cl:11])[CH:6]=2)(=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 114 employing 3-amino-2-benzoyl-6-chloroindole (Example 1) and cyclopropylacetic acid. m.p.: 72-75° C.
Sources & evidence
- ORD record
- ord-bf886feb30fa47429ed0a121580390c7
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06300363B1
Reaction notes
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