Piperazine → 2-Piperazin-1-yl-thiazole-5-carbonitrile
Reaction equation
Cl[C:2]1[S:3][C:4]([C:7]#[N:8])=[CH:5][N:6]=1.[NH:9]1[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1>>[N:9]1([C:2]2[S:3][C:4]([C:7]#[N:8])=[CH:5][N:6]=2)[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1Participants
3
Procedure
Prepared in analogy to example 2 (b) from 2-chloro-1,3-thiazole-5-carbonitrile and piperazine. The crude material was purified by chromatography (SiO2, methanol/dichloromethane) to yield the title compound as a white crystalline solid (yield 86%). MS (m/e): 194.9 (M+H+, 100%).
Workup
- customThe crude material was purified by chromatography (SiO2, methanol/dichloromethane)
Sources & evidence
- ORD record
- ord-fce90215517c4860b1f7ec6872b1e808
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07220744B2
Reaction notes
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