Methylamine → HCID 178482611, compound
Reaction equation
Br[CH2:2][C:3]1[CH:18]=[CH:17][C:6]2[N:7]=[C:8]([C:10]3[C:14]([CH3:15])=[N:13][NH:12][C:11]=3[NH2:16])[S:9][C:5]=2[CH:4]=1.[CH3:19][NH2:20]>>[CH3:15][C:14]1[C:10]([C:8]2[S:9][C:5]3[CH:4]=[C:3]([CH2:2][NH:20][CH3:19])[CH:18]=[CH:17][C:6]=3[N:7]=2)=[C:11]([NH2:16])[NH:12][N:13]=1Participants
3
Procedure
The title compound (1.6 mg) was prepared starting from 18 mg of 4-(6-bromomethylbenzothiazol-2-yl)-5-methyl-2H-pyrazol-3-ylamine and excess methylamine. MS (m/z, ES+): 274.1 (M+1,100%), 243.1 (M−CH3NH, 60%).
Sources & evidence
- ORD record
- ord-a1ad4e3fc72249c8974155b3c415e1ca
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09434720B2
Reaction notes
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