Aminoacetaldehyde dimethyl acetal → 8-Chloro-7-methylisoquinoline

HRID 461480Notes

Reaction equation

HRID 461480 reaction equation
[Cl:1][C:2]1[C:9]([CH3:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.CO[CH:13](OC)[CH2:14][NH2:15]>>[Cl:1][C:2]1[C:9]([CH3:10])=[CH:8][CH:7]=[C:6]2[C:3]=1[CH:4]=[N:15][CH:14]=[CH:13]2

Participants

3

Reactant 2

HCID 89728Aminoacetaldehyde dimethyl acetalHCID 144927792-Chloro-3-methylbenzaldehyde

Product 1

HCID 213938078-Chloro-7-methylisoquinoline

Procedure

8-Chloro-7-methylisoquinoline was prepared from 2-chloro-3-methylbenzaldehyde and 2,2-dimethoxyethylamine by the procedure described in Example 1.

Sources & evidence

ORD record
ord-c3ef557a22b641fa9d9c8d2c1219d89a
Source dataset
uspto-grants-1977_12
Patent number
US04062961

Reaction notes

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