HCID 19803458, compound → HCID 67917832, compound

HRID 1682076Notes

Reaction equation

HRID 1682076 reaction equation
[NH:1]1[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]([CH2:8][N:9]2[C:15](=[O:16])[CH2:14][C:13]3[CH:17]=[C:18]4[O:23][CH2:22][O:21][C:19]4=[CH:20][C:12]=3[CH2:11][CH2:10]2)[CH2:2]1.C1(S(O[CH2:34][CH2:35][CH2:36][C:37]2[C:45]3[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=3)[NH:39][CH:38]=2)(=O)=O)C=CC=CC=1>>[OH2:16].[NH:39]1[C:40]2[C:45](=[CH:44][CH:43]=[CH:42][CH:41]=2)[C:37]([CH2:36][CH2:35][CH2:34][N:1]2[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]([CH2:8][N:9]3[C:15](=[O:16])[CH2:14][C:13]4[CH:17]=[C:18]5[O:23][CH2:22][O:21][C:19]5=[CH:20][C:12]=4[CH2:11][CH2:10]3)[CH2:2]2)=[CH:38]1

Participants

3

Reactant 2

HCID 19803458HCID 19803458, compoundHCID 19803590HCID 19803590, compound

Product 1

HCID 67917832HCID 67917832, compound

Procedure

Prepared from 3-[(hexahydro-azepin-3-yl)-methyl]-7,8-methylenedioxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepin and 3-(3-benzenesulphonyloxy-propyl)-indole analogously to Example 1.

Sources & evidence

ORD record
ord-1c47fcff65a64a9da52028423c22e2c6
Source dataset
uspto-grants-1992_12
Patent number
US05175157

Reaction notes

Loading…