HCID 17804786, compound → HCID 19804052, compound

HRID 1682028Notes

Reaction equation

HRID 1682028 reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][CH:3]([CH2:7][CH2:8][N:9]2[CH2:18][CH2:17][C:16]3[C:11](=[CH:12][C:13]([O:21][CH3:22])=[C:14]([O:19][CH3:20])[CH:15]=3)[C:10]2=[O:23])[CH2:2]1.[Cl:24][CH2:25][CH2:26][CH2:27][O:28][C:29]1[C:34]2[O:35][CH2:36][O:37][C:31](=[CH:32][CH:33]=2)[CH:30]=1>>[ClH:24].[CH2:36]1[O:35][C:32]2[CH:33]=[CH:34][C:29]([O:28][CH2:27][CH2:26][CH2:25][N:1]3[CH2:6][CH2:5][CH2:4][CH:3]([CH2:7][CH2:8][N:9]4[CH2:18][CH2:17][C:16]5[C:11](=[CH:12][C:13]([O:21][CH3:22])=[C:14]([O:19][CH3:20])[CH:15]=5)[C:10]4=[O:23])[CH2:2]3)=[CH:30][C:31]=2[O:37]1

Participants

3

Reactant 2

HCID 17804786HCID 17804786, compoundHCID 19803906HCID 19803906, compound

Product 1

HCID 19804052HCID 19804052, compound

Procedure

Prepared from 2-[(piperidin-3-yl)-ethyl]-6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-chloro-3-(3,6-methylenedioxy-phenoxy)-propane analogously to Example 1.

Sources & evidence

ORD record
ord-031467afd731473c82f3db7ae621b3ba
Source dataset
uspto-grants-1992_12
Patent number
US05175157

Reaction notes

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