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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655583Generated: October 29, 2026

Hydrochloric Acid → HCID 44612367, compound

https://huagongshe.com/reaction/655583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Chloro-4-fluorophenyl isocyanateHCID 2734632—
ReactantHCID 68538825HCID 68538825—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 44612367HCID 4461236795.1%

Reaction Steps

A solution of (S)-4-[(S)-3-((S)-4-hydroxy-6-aza-spiro[2.5]oct-6-yl)-1-methoxymethyl-propyl]-2-methyl-3-oxo-piperazine-1-carboxylic acid tert-butyl ester (intermediate 23; 47 mg, 0.11 mmol) in 1,4-dioxane (0.5 mL) was cooled to 0° C. and treated with hydrogen chloride solution (4 M in 1,4-dioxane, 0.28 mL, 1.1 mmol) The ice bath was removed, the reaction mixture stirred for 4 h, then 4-methylmorpholine (112 mg, 1.1 l mmol) and N,N-dimethylformamide (1 mL) were added. To this reaction mixture was added 3-chloro-4-fluorophenyl isocyanate (19 mg 0.11 mmol), then after 16 h the reaction mixture was partitioned between water and ethyl acetate. The aqueous layer was saturated with sodium chloride and extracted with ethyl acetate. The combined organic phases were dried (MgSO4), filtered, and evaporated. Chromatography (SiO2; dichloromethane/methanol/25% aq. ammonia solution gradient 98:2:0.25 to 90:10:0.25) furnished the title compound (52 mg, 95%). Light yellow gum, MS (ISP)=497.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071586B2
Source datasetuspto-grants-2011_12
ORD IDord-a173015411574d7dae112bf97bec55a1
Source noteuspto-grants-2011_12