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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626102Generated: November 1, 2026

Hydrochloric Acid → HCID 71008948, compound

https://huagongshe.com/reaction/1626102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 71009123HCID 71009123—
SolventMethanolHCID 887—
ProductHCID 71008948HCID 7100894896.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (R)-2-methyl-propane-2-sulfinic acid {(R)-1-[1-(3-bromo-phenyl)-1H-pyrazol-4-yl]-2,2-difluoro-3-hydroxy-1-methyl-propyl}-amide (590 mg, 1.2 mmol) in methanol (5 ml) was treated at 0° C. with hydrochloric acid (4N in dioxane, 2.6 ml, 10.2 mmol), and the reaction mixture was stirred at 25° C. for 2 hours. For the workup, the solution was concentrated at reduced pressure, and the resultant residue was diluted with water (10 ml). The aqueous layer was treated with a saturated solution of sodium hydrogencarbonate to a pH of about 8, then extracted with ethyl acetate (4×10 ml). The combined organic layers were washed with brine (15 ml), dried over sodium sulphate, and evaporated at reduced pressure. The crude material thus obtained was purified by column chromatography on silica gel using a gradient of hexane/ethyl acetate=85:15 to 80:20 as the eluent to give the (R)-3-amino-3-[1-(3-bromo-phenyl)-1H-pyrazol-4-yl]-2,2-difluoro-butan-1-ol (400 mg, 96% yield) as a light yellow solid which was used in the next step without further purification. MS (ISP): m/z=346.5 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785436B2
Source datasetuspto-grants-2014_07
ORD IDord-1ac8f84decee4599a70d541a56f107b5
Source noteuspto-grants-2014_07