HCID 14306655, compound → HCID 19803958, compound

HRID 1682042Notes

Reaction equation

HRID 1682042 reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][CH:3]([CH2:7][N:8]2[CH2:17][CH2:16][C:15]3[C:10](=[CH:11][C:12]([O:20][CH3:21])=[C:13]([O:18][CH3:19])[CH:14]=3)[C:9]2=[O:22])[CH2:2]1.[Cl:23][CH2:24][CH2:25][CH2:26][N:27]([C:29]1[CH:34]=[CH:33][C:32]([O:35][CH3:36])=[CH:31][CH:30]=1)[CH3:28]>>[ClH:23].[ClH:23].[CH3:36][O:35][C:32]1[CH:33]=[CH:34][C:29]([N:27]([CH2:26][CH2:25][CH2:24][N:1]2[CH2:6][CH2:5][CH2:4][CH:3]([CH2:7][N:8]3[CH2:17][CH2:16][C:15]4[C:10](=[CH:11][C:12]([O:20][CH3:21])=[C:13]([O:18][CH3:19])[CH:14]=4)[C:9]3=[O:22])[CH2:2]2)[CH3:28])=[CH:30][CH:31]=1

Participants

3

Reactant 2

HCID 14306655HCID 14306655, compoundHCID 19803564HCID 19803564, compound

Product 1

HCID 19803958HCID 19803958, compound

Procedure

Prepared from 2-[(piperidin-3-yl)-methyl]-6,7-dimethoxy- 1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-chloro-3-(4-methoxy-N-methyl-phenylamino)-propane analogously to Example 1.

Sources & evidence

ORD record
ord-ede08982bf4744bfbd5ee246e0daffe3
Source dataset
uspto-grants-1992_12
Patent number
US05175157

Reaction notes

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