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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409393Generated: November 2, 2026

Sodium borohydride → HCID 86714652, compound

https://huagongshe.com/reaction/1409393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 70981912HCID 70981912—
SolventMethanolHCID 887—
ProductHCID 86714652HCID 86714652—

Reaction Steps

(S)-2-Acetyl-N-(1-(3-(3-chloro-4-cyano-5-fluorophenyl)-1H-pyrazol-1-yl)-propan-2-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-4-carboxamide (290 mg, 0.53 mmol) was dissolved in MeOH (20 ml). NaBH4 (30 mg, 0.79 mmol) was added to the solution in portions at 0° C. and the mixture was stirred at RT for 3 h. The reaction mixture was concentrated and dluted with water. The mixture was extracted with DCM and the organic layer was concentrated. The product was purified by column chromatography. Yield 245 mg. 1H-NMR (400 MHz; DMSO-d6): δ −0.05 (s, 9H), 0.81-0.86 (m, 2H), 1.07-1.1 (m, 3H), 1.49 (d, 3H), 3.47-3.51 (m, 2H), 4.29-4.43 (m, 3H), 4.88-4.91 (m, 1H), 5.4-5.45 (m, 3H), 7.03 (d, 1H), 7.68 (d, 1H), 7.86-8.00 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921378B2
Source datasetuspto-grants-2014_12
ORD IDord-4b4415ed5fa24eefbbdb8b0342b6553f
Source noteuspto-grants-2014_12