Hydrogen Bromide → HCID 68988307, compound

HRID 69448Notes

Reaction equation

HRID 69448 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([N:16]2[CH2:25][CH2:24][C:23]3[C:18](=[CH:19][CH:20]=[C:21]([O:26]C)[CH:22]=3)[C:17]2=[O:28])[CH:5]=[CH:6][C:7]=1[N:8]1[CH2:12][CH2:11][CH:10]([N:13]([CH3:15])[CH3:14])[CH2:9]1.Br>>[Cl:1][C:2]1[CH:3]=[C:4]([N:16]2[CH2:25][CH2:24][C:23]3[C:18](=[CH:19][CH:20]=[C:21]([OH:26])[CH:22]=3)[C:17]2=[O:28])[CH:5]=[CH:6][C:7]=1[N:8]1[CH2:12][CH2:11][CH:10]([N:13]([CH3:15])[CH3:14])[CH2:9]1

Participants

3

Procedure

According to Method L, 2-[3-chloro-4-(3-dimethylamino-pyrrolidin-1-yl)-phenyl]-6-methoxy-3,4-dihydro-2H-isoquinolin-1-one was treated with hydrogen bromide. In this way the product was obtained with molecular weight 385.90 (C21H24ClN3O2); MS (ESI): 386 (M+H+).

Workup

  1. customIn this way the product was obtained with molecular weight 385.90 (C21H24ClN3O2)

Sources & evidence

ORD record
ord-92eace72f613402b9abd19f7f271eb67
Source dataset
uspto-grants-2014_09
Patent number
US08822495B2

Reaction notes

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