1-Chloromethyl-2-methylnaphthalene → HCID 19803655, compound

HRID 1682025Notes

Reaction equation

HRID 1682025 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][C:25]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH:28]=[CH:27][C:26]=1[CH3:35]>>[ClH:23].[CH3:35][C:26]1[CH:27]=[CH:28][C:29]2[C:34](=[CH:33][CH:32]=[CH:31][CH:30]=2)[C:25]=1[CH2:24][N: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

Participants

3

Reactant 2

HCID 811061-Chloromethyl-2-methylnaphthaleneHCID 14306655HCID 14306655, compound

Product 1

HCID 19803655HCID 19803655, compound

Procedure

Prepared from 2-[(piperidin-3-yl)-methyl]-6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydro-isoquinoline and 1-chloromethyl-2-methyl-naphthalene analogously to Example 1.

Sources & evidence

ORD record
ord-89c43aaf981b4078a3fe12c0ef55e047
Source dataset
uspto-grants-1992_12
Patent number
US05175157

Reaction notes

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