2-Methoxybenzoyl chloride → HCID 18687378, compound

HRID 1872711Notes

Reaction equation

HRID 1872711 reaction equation
[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][N:6]([CH3:12])[CH2:7]2.[CH3:13][O:14][C:15]1[CH:23]=[CH:22][CH:21]=[CH:20][C:16]=1[C:17]([Cl:19])=[O:18]>>[ClH:19].[CH3:12][N:6]1[CH2:5][CH2:4][C:3]2[C:8](=[CH:9][CH:10]=[CH:11][C:2]=2[NH:1][C:17](=[O:18])[C:16]2[CH:20]=[CH:21][CH:22]=[CH:23][C:15]=2[O:14][CH3:13])[CH2:7]1

Participants

3

Reactant 2

HCID 889692-Methoxybenzoyl chlorideHCID 141712692-Methyl-1,2,3,4-tetrahydroisoquinolin-5-amine

Product 1

HCID 18687378HCID 18687378, compound

Procedure

The title compound was prepared in an analogous fashion to Example 2 from 5-amino-2-methyl-1,2,3,4-tetrahydroisoquinoline and 2-methoxybenzoyl chloride.

Sources & evidence

ORD record
ord-c4954631fca24fdc94328ca1de21973e
Source dataset
uspto-grants-2000_08
Patent number
US06110934

Reaction notes

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