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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487463Generated: October 31, 2026

Hydrochloric Acid → HCID 86695421, compound

https://huagongshe.com/reaction/1487463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantMethylamineHCID 6329—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86695419HCID 86695419—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86695421HCID 8669542132.8%

Reaction Steps

Mesyl anhydride (860 mg, 4.9 mmol) is added to 2,2-difluoro-1-((4S,5R)-4-(fluoromethyl)-5-(4-(2-(hydroxymethyl)thiazol-5-yl)phenyl)-2,2-dimethyl-oxazolidin-3-yl)ethanone (1.4 g, 3.5 mmol) in CH2Cl2 (35 mL). Pyridine (0.5 mL, 5.9 mmol) is added and stirred at room temperature for 1 hour. The reaction is diluted with CH2Cl2 (35 mL) and washed with water and brine. The organic phase is dried (Na2SO4) and concentrated under vacuum. The crude mesylate is dissolved in acetonitrile (10 mL) and transferred to a scintillation vial. Diisopropylethylamine (0.65 mL, 3.7 mmol) and methylamine.HCl (130 mg, 1.9 mmol) are added and the reaction mixture is heated to 55° C. for 18 hours. The reaction mixture is cooled and diluted with saturated NaHCO3 (75 mL). The reaction mixture is extracted with CH2Cl2 (2×75 mL) and the combined organic phase is dried (Na2SO4) and concentrated under vacuum to afford the title compound (475 mg): m/z (CI) M+H 414.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428528B2
Source datasetuspto-grants-2016_08
ORD IDord-41a3de86776b4b71a0a7effc1ef8e5d6
Source noteuspto-grants-2016_08