Ammonia → HCID 57655924, compound

HRID 2041442Notes

Reaction equation

HRID 2041442 reaction equation
Br[CH2:2][C:3]1[CH:17]=[CH:16][C:6]2[N:7]=[C:8]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[S:9][C:5]=2[CH:4]=1.[NH3:18]>CO>[NH2:18][CH2:2][C:3]1[CH:17]=[CH:16][C:6]2[N:7]=[C:8]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[S:9][C:5]=2[CH:4]=1

Participants

4

Procedure

Add 6-bromomethyl-2-phenyl-benzothiazole (2 g, 6.57 mmol) as a suspension in methanol (100 mL) to 7M ammonia in methanol (400 mL) at 0° C. over 10 min and then stir for 3 h at room temperature. Concentrate in vacuo and purify the crude mixture by chromatography on silica gel eluting with dichloromethane/methanol (1:0 to 3:1) to obtain the title compound (1.2 g, 76%). MS (ES+) m/z: 241 (M+H+).

Workup

  1. concentrationConcentrate in vacuo
  2. custompurify the crude mixture by chromatography on silica gel eluting with dichloromethane/methanol (1:0 to 3:1)

Sources & evidence

ORD record
ord-a5db8cb369994eb491723e64fcde8602
Source dataset
uspto-grants-2013_11
Patent number
US08580780B2

Reaction notes

Loading…