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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171909Generated: October 25, 2026

Bromide ion → (S)-2-(2-benzyl-4-(3-(cyclopentyloxy)-4-methoxyphenyl)piperazin-1-yl)acetamide

https://huagongshe.com/reaction/1171909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant2-BromoacetamideHCID 69632—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazineHCID 16725642—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-(2-benzyl-4-(3-(cyclopentyloxy)-4-methoxyphenyl)piperazin-1-yl)acetamideHCID 23627744—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of the bishydrochloride salt of (S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazine (Example 2) (110 mg, 0.25 mmol) in THF (2 mL) at room temperature was treated with diisopropylethylamine (165 μL, 1.0 mmol) followed by 2-bromoacetamide (42 mg, 0.3 mmol). The reaction mixture was heated at 50° C. for 8 h and an additional amount of bromide (42 mg, 0.3 mmol) then added. The reaction mixture was then stirred for an additional 16 h at room temperature and evaporated. The crude reaction was then partitioned between EtOAc (3 mL) and a saturated aqueous NaHCO3 solution (3 mL). The organic phase was isolated and further washed with an additional portion of a saturated aqueous NaHCO3 solution (3 mL) and brine (2×3 mL).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829713B2
Source datasetuspto-grants-2010_11
ORD IDord-0b82a7b66e454e84ad26c5a1854d51e6
Source noteuspto-grants-2010_11