Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089446Generated: October 31, 2026

Sodium borohydride → HCID 67439041, compound

https://huagongshe.com/reaction/2089446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58464861HCID 58464861—
SolventMethanolHCID 887—
ProductHCID 67439041HCID 6743904185%

Reaction Steps

tert-Butyl 2-(2,6-difluorophenyl)-4-(1-methyl-5-(4-oxocyclohexyl)-1H-pyrazol-4-ylcarbamoyl)thiazol-5-ylcarbamate (68 mg, 0.13 mmol) was dissolved in methanol (3 mL) and sodium borohydride (16 mg, 0.39 mmol) was added. The mixture was stirred at RT for 30 min then quenched with sat. NaHCO3 and extracted with ethyl acetate three times. Combined organic layers were dried over sodium sulfate, filtered and concentrated to give the crude tert-butyl 2-(2,6-difluorophenyl)-4-(5-(4-hydroxycyclohexyl)-1-methyl-1H-pyrazol-4-ylcarbamoyl)thiazol-5-ylcarbamate (58 mg, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436001B2
Source datasetuspto-grants-2013_05
ORD IDord-578fef0a72b54071b56427ab2a2cc431
Source noteuspto-grants-2013_05