HCID 19803964, compound → HCID 67918369, compound

HRID 1682072Notes

Reaction equation

HRID 1682072 reaction equation
[CH2:1]1[O:15][C:4]2[CH:5]=[CH:6][C:7]3[CH2:8][C:9](=[O:14])[NH:10][CH2:11][CH2:12][C:13]=3[C:3]=2[O:2]1.[CH3:16][O:17][C:18]1[CH:36]=[CH:35][C:21]([O:22][CH2:23][CH2:24][CH2:25][N:26]2[CH2:32][CH2:31][CH2:30][CH2:29][CH:28]([CH2:33][Cl:34])[CH2:27]2)=[CH:20][CH:19]=1>>[ClH:34].[CH3:16][O:17][C:18]1[CH:19]=[CH:20][C:21]([O:22][CH2:23][CH2:24][CH2:25][N:26]2[CH2:32][CH2:31][CH2:30][CH2:29][CH:28]([CH2:33][N:10]3[C:9](=[O:14])[CH2:8][C:7]4[CH:6]=[CH:5][C:4]5[O:15][CH2:1][O:2][C:3]=5[C:13]=4[CH2:12][CH2:11]3)[CH2:27]2)=[CH:35][CH:36]=1

Participants

3

Reactant 2

HCID 19803964HCID 19803964, compoundHCID 19804140HCID 19804140, compound

Product 1

HCID 67918369HCID 67918369, compound

Procedure

Prepared from 6,7-methylenedioxy-2-oxo-1,3,4,5-tetrahydro-2H-3-benzazepine and N-[3-(4-methoxy-phenoxy)-propyl]-3-chloromethylhexahydro-azepine analogously to Example 2.

Sources & evidence

ORD record
ord-4432d4448ad74fea9ce86ee8b954567a
Source dataset
uspto-grants-1992_12
Patent number
US05175157

Reaction notes

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