HCID 19800277, compound → HCID 19800246, compound
Reaction equation
[ClH:1].[C:2]1([C:8]2[C:9]([S:17]([C:20]3[CH:25]=[CH:24][C:23]([O:26][CH2:27][CH2:28][CH2:29][NH:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[C:22](C)[CH:21]=3)(=[O:19])=[O:18])=[C:10]3[N:15]([CH:16]=2)[CH:14]=[CH:13][CH:12]=[CH:11]3)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>CO>[ClH:1].[C:2]1([C:8]2[C:9]([S:17]([C:20]3[CH:21]=[CH:22][C:23]([O:26][CH2:27][CH2:28][CH2:29][NH:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[CH:24][CH:25]=3)(=[O:18])=[O:19])=[C:10]3[N:15]([CH:16]=2)[CH:14]=[CH:13][CH:12]=[CH:11]3)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
2-Phenyl-1-{4-[3-(tert-butylamino)propyloxy]-3-methylbenzenesulphonyl}indolizine hydrochloride (SR 33485 A) (Example 25) M.p. b 181° C. (methanol)
Sources & evidence
- ORD record
- ord-b69cf5a466614dd39579c423c72e2782
- Source dataset
- uspto-grants-1990_09
- Patent number
- US04957925
Reaction notes
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