Acetyl chloride → HCID 18368143, 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]([CH:14]1[CH2:19][CH2:18][CH2:17][CH:16]([CH3:20])[CH2:15]1)=[O:13].[C:21](Cl)(=[O:23])[CH3:22]>C(OCC)(=O)C.CCCCCC>[C:21]([NH: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]([CH:14]1[CH2:19][CH2:18][CH2:17][CH:16]([CH3:20])[CH2:15]1)=[O:13])(=[O:23])[CH3:22]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared according to the procedure described in Example 19 employing 3-amino-6-chloro-2-(3-methylcyclohexylcarbonyl)indole (Example 144) and acetyl chloride. m.p.: 202-203° C. (ethyl acetate/hexane)
Sources & evidence
- ORD record
- ord-e00bc63b49e04c96963ad60b9fdd0fc6
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06300363B1
Reaction notes
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