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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-ethyl-4-methyl-1H-pyrazol-5-amine | HCID 3134941 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 178432774 | HCID 178432774 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178437903 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835444B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-34cf35e4dbf04b429917dc488efcea35 |
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| Source note | uspto-grants-2014_09 |
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