Stannous Chloride → Ethyl 3-(3-[3-aminophenylsulphonylamino]-phenyl)-3-(2-phenylbutyrylamino)propionate

HRID 1596581Notes

Reaction equation

HRID 1596581 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([S:10]([NH:13][C:14]2[CH:15]=[C:16]([CH:20]([NH:27][C:28](=[O:38])[CH:29]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)[CH2:30][CH3:31])[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH:17]=[CH:18][CH:19]=2)(=[O:12])=[O:11])[CH:7]=[CH:8][CH:9]=1)([O-])=O.[Sn](Cl)Cl>>[NH2:1][C:4]1[CH:5]=[C:6]([S:10]([NH:13][C:14]2[CH:15]=[C:16]([CH:20]([NH:27][C:28](=[O:38])[CH:29]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)[CH2:30][CH3:31])[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH:17]=[CH:18][CH:19]=2)(=[O:11])=[O:12])[CH:7]=[CH:8][CH:9]=1

Participants

3

Procedure

Corresponding to Example 3d, 5 g of (7c) were treated with tin-(II) chloride. A yellowish solid was obtained (yield: 1.8 g).

Workup

  1. customA yellowish solid was obtained (yield: 1.8 g)

Sources & evidence

ORD record
ord-4abe6e460e134b13bc2736c5b022cb9b
Source dataset
uspto-grants-2001_09
Patent number
US06291503B1

Reaction notes

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