2-Amino-4,5,6,7-tetrahydrobenzothiazole → 3-(2-methoxy-ethyl)-4,5,6,7-tetrahydro-3H-benzothiazol-2-ylideneamine hydrobromide

HRID 78423

Reaction equation

HRID 78423 reaction equation
[S:1]1[C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:4]=2[N:3]=[C:2]1[NH2:10].[CH3:11][O:12][CH2:13][CH2:14][Br:15]>>[BrH:15].[CH3:11][O:12][CH2:13][CH2:14][N:3]1[C:4]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[S:1][C:2]1=[NH:10]

Participants

3

Procedure

A mixture of 4,5,6,7-tetrahydro-benzothiazol-2-ylamine (300 mg, 1.94 mmol) and 2-bromoethyl methyl ether (600 μL, 6.40 mmol) was processed according to the method of Example 12A to provide the title compound as crude product: MS (LC/MS) m/z 213 (M+H)+.

Sources & evidence

ORD record
ord-8847ec3281d5466a99cd84ae68050294
Source dataset
uspto-grants-2014_09
Patent number
US08841334B2

Linked notes

Loading…