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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411255Generated: October 30, 2026

Acetone → (2R)-1-[4-[3-[4-(Cyclopropylcarbonyl)phenoxy]propyl]-1-piperazinyl]-2-[(1-methylethyl)amino]-1-propanone

https://huagongshe.com/reaction/411255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantA 304121HCID 9906860—
Product(2R)-1-[4-[3-[4-(Cyclopropylcarbonyl)phenoxy]propyl]-1-piperazinyl]-2-[(1-methylethyl)amino]-1-propanoneHCID 4430405625%

Reaction Steps

Sodium cyanoborohydride (75 mg, 1.2 mmol) was added to a room temperature solution of Example 138 (401 mg, 1 mmol) in acetone (10 mL). After stirring overnight, the reaction mixture was concentrated, and the concentrate was taken up in dichloromethane and washed with water, and brine, dried (Na2SO4), filtered, concentrated and purified by silica gel column chromatography using dichloromethane:methanol (9:1) as the eluant. The product was obtained in 25% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559140B2
Source datasetuspto-grants-2003_05
ORD IDord-d6ad7b7576454d32909299eead388320
Source noteuspto-grants-2003_05