1-Cyclopropyl-4-nitro-1H-pyrazole → 1-Cyclopropyl-1H-pyrazol-4-amine
Reaction equation
[CH:1]1([N:4]2[CH:8]=[C:7]([N+:9]([O-])=O)[CH:6]=[N:5]2)[CH2:3][CH2:2]1>C(O)C>[CH:1]1([N:4]2[CH:8]=[C:7]([NH2:9])[CH:6]=[N:5]2)[CH2:3][CH2:2]1Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A 250-mL Parr reactor bottle was purged with nitrogen and charged with 10% palladium on carbon (50% wet, 117 mg dry weight) and a solution of 109a (500 mg, 6.73 mmol) in ethanol (36 mL). The bottle was attached to a Parr hydrogenator, evacuated, charged with hydrogen gas to a pressure of 50 psi and shaken for 2 h. After this time, the hydrogen was evacuated, and nitrogen was charged into the bottle. Celite 521 (1.00 g) was added, and the mixture was filtered through a pad of Celite 521. The filter cake was washed with ethanol (2×25 mL), and the combined filtrates were concentrated to dryness under reduced pressure to afford a 94% yield of 109b (378 mg) as a purple oil: 1H NMR (300 MHz, CDCl3) δ 7.13 (s, 1H), 7.07 (s, 1H), 3.47 (m, 1H), 2.87 (br s, 2H), 0.96 (m, 4H); MS (ESI+) m/z 124.1 (M+H).
Workup
- customA 250-mL Parr reactor bottle was purged with nitrogen
- additioncharged with 10% palladium on carbon (50% wet, 117 mg dry weight)
- customevacuated
- additioncharged with hydrogen gas to a pressure of 50 psi
- customAfter this time, the hydrogen was evacuated
- additionnitrogen was charged into the bottle
- additionCelite 521 (1.00 g) was added
- filtrationthe mixture was filtered through a pad of Celite 521
- washThe filter cake was washed with ethanol (2×25 mL)
- concentrationthe combined filtrates were concentrated to dryness under reduced pressure
Sources & evidence
- ORD record
- ord-4b8047a3a1414016a7ccdcc691c58f5d
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09249123B2
Reaction notes
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