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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75499Generated: October 29, 2026

3-ethyl-4-methyl-1H-pyrazol-5-amine → HCID 178437903, compound

https://huagongshe.com/reaction/75499

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ethyl-4-methyl-1H-pyrazol-5-amineHCID 3134941—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178432774HCID 178432774—
SolventDichloromethaneHCID 6344—
ProductHCID 178437903HCID 178437903—

Reaction Steps

A mixture comprising trans-5-chloro-N-(4-formyl-cyclohexyl)-2-methyl-nicotinamide Intermediate E) (100 mg, 0.30 mmol) and 5-ethyl-4-methyl-1H-pyrazol-3-amine (37.5 mg, 0.30 mmol) in DCM (5 ml) was treated with sodium triacetoxyborohydride (95 mg, 0.45 mmol). The reaction mixture was stirred at RT for 18 hours and then partitioned between DCM and sat. NaHCO3. The organic phase was passed through a phase separator and the solvent was removed in vacuo. The resulting crude product was triturated in EtOAc, filtered and dried to afford the title compound; 1H NMR (d6-DMSO, 400 MHz) δ 10.87 (1H, s), 8.53 (1H, m), 8.40 (1H, m), 7.80 (1H, m), 4.43 (1H, m), 3.69 (1H, m), 2.90 (2H, t), 2.50 (3H, s), 2.40 (2H, q), 1.88 (4H, m), 1.73 (3H, s), 1.53 (1H, m), 1.21 (2H, m), 1.09 (3H, t), 1.00 (2H, m); LCMS Rt=2.06 min, [M+H]+390 Method LowpH_v002.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835444B2
Source datasetuspto-grants-2014_09
ORD IDord-34cf35e4dbf04b429917dc488efcea35
Source noteuspto-grants-2014_09