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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006340Generated: October 30, 2026

Dichloromethane → HCID 69819820, compound

https://huagongshe.com/reaction/1006340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSulfur, trifluoro(N-methylmethanaminato)-HCID 123203—
ReactantAcetone cardiceHCID 18522661—
ReactantHCID 86589645HCID 86589645—
ProductHCID 69819820HCID 69819820—

Reaction Conditions

Temperature-50 °C

Reaction Steps

(Dimethylamino)sulfur trifluoride (0.068 ml) was added dropwise to a solution of tert-butyl (4R,7R,8aS)-4-benzhydryl-7-hydroxyhexahydropyrrolo[1,2-a]pyrazine-2(1H)-carboxylate (115 mg) in dichloromethane (2 ml) under cooling with dry ice-acetone. The mixture was stirred for 20 minutes at the same temperature (−50° C.), followed by room temperature for 2 hours. The mixture was poured into ice-water and the dichloromethane layer was separated, dried over magnesium sulfate, and evaporated under reduced pressure. The syrup was purified by column chromatography on silica gel using a mixed solvent of hexane and ethyl acetate (2:1). The fractions containing the objective compound were collected and evaporated under reduced pressure. The resulting syrup was treated with 4N hydrogen chloride in ethyl acetate (2 ml) and evaporated under reduced pressure to give (4R,7S,8aS)-4-benzhydryl-7-fluorooctahydropyrrolo[1,2-a]pyrazine dihydrochloride (75 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787543B2
Source datasetuspto-grants-2004_09
ORD IDord-1dcbec091ee6440488bc0888f507b957
Source noteuspto-grants-2004_09