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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388902Generated: October 30, 2026

Hydrochloric Acid → HCID 59558799, compound

https://huagongshe.com/reaction/2388902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantAzetidine hydrochlorideHCID 12308726—
ReactantHCID 53628422HCID 53628422—
ReactantHCID 67051257HCID 67051257—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 59558799HCID 59558799—

Reaction Steps

Azetidine hydrochloride (0.11 g) was added to a solution of acetic acid (0.025 mL) and N-{2-[(2,3-difluorobenzyl)thio]-6-methoxypyrimidin-4-yl}-4-oxopiperidine-1-sulfonamide (the product of example 148, step (0.10 g) in DCM (4 mL). The solution was stirred at room temperature for 1 h then sodium triacetoxyborohydride (0.24 g) was added in portions. The mixture was stirred at room temperature overnight then 3M aqueous sodium hydroxide (6 mL) added to the residue. The mixture was shaken vigorously then acidified to pH 8 with 2 M aqueous hydrochloric acid and extracted with ethyl acetate. The combined organic extracts were concentrated then methanol (1 mL) was added and the resulting suspension filtered. The solid was washed with water, methanol and ethyl acetate to afford the title compound as a white powder. Yield: 47 mg

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269002B2
Source datasetuspto-grants-2012_09
ORD IDord-6b34f7a5ae524fc69f38d995c76d47d8
Source noteuspto-grants-2012_09