Dimethylamine → HCID 178483399, compound
Reaction equation
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[C:14]([CH2:15][CH2:16][CH2:17]Br)=[N:13][NH:12][C:11]=1[NH2:19].NC1NN=C(CCCO)C=1[C:30]1SC2C=CC=C[C:33]=2[N:34]=1.CNC.C1COCC1>>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[C:14]([CH2:15][CH2:16][CH2:17][N:34]([CH3:33])[CH3:30])=[N:13][NH:12][C:11]=1[NH2:19]Participants
5
Procedure
The title compound (100 mg) was prepared using 200 mg (0.59 mmol) of 4-benzothiazol-2-yl-5-(3-bromopropyl)-2H-pyrazol-3-ylamine, which was derived from 3-(5-amino-4-benzothiazol-2-yl-1H-pyrazol-3-yl)-propan-1-ol, and 5 mL of a 2 M solution of dimethylamine in THF (10 mmol). MS (m/z, ES+): 302.1 (M+1, 100%).
Sources & evidence
- ORD record
- ord-579e16a7f5b748e695b1eff61f0dab3d
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754233B2
Reaction notes
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