Propionyl chloride → HCID 18368074, compound
Reaction equation
[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[N:4]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:3]=1[C:17](=[O:25])[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([Cl:24])[CH:19]=1.[C:26](Cl)(=[O:29])[CH2:27][CH3:28]>>[Cl:11][C:7]1[CH:6]=[C:5]2[C:10]([C:2]([NH:1][C:26](=[O:29])[CH2:27][CH3:28])=[C:3]([C:17](=[O:25])[C:18]3[CH:23]=[CH:22][CH:21]=[C:20]([Cl:24])[CH:19]=3)[N:4]2[C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:9][CH:8]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in step 1 of Example 2 (Method A) from 3-amino-6-chloro-2-(3-chlorobenzoyl)-1-(ethoxycarbonyl)indole (step 1 of Example 30) and propionyl chloride.
Sources & evidence
- ORD record
- ord-b3861f134b1a4075bcfddce856387daa
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06300363B1
Reaction notes
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