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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986962Generated: November 2, 2026

Borohydride → HCID 10299314, compound

https://huagongshe.com/reaction/1986962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorohydrideHCID 28123—
Reactant1H-Imidazole-1-propanamineHCID 78736—
ReactantHCID 86591120HCID 86591120—
SolventDichloromethaneHCID 6344—
ProductHCID 10299314HCID 10299314—

Reaction Steps

A solution of (1R,2R)-2-[4-(6-Trifluoromethyl-benzo[b]thiophen-3-yl)-piperazin-1-ylmethyl]-cyclopropanecarbaldehyde (36.8 mg, 0.1 mmol) and 1-(3-aminopropyl)imidazole (0.0235 ml, 2.1 mmol) in anhydrous methylene chloride (3 ml) is added to a solution of polymer supported borohydride (0.863 g, 3 mmol) soaked in anhydrous methylene chloride (4 ml). This mixture was shook on an orbital shaker at room temperature overnight. The reaction was then quenched with water (2 ml) and products extracted with ethyl acetate (10 ml), then washed with brine, dried with sodium sulfate, and concentrated in vacuo. Silica gel chromatography eluted with methylene chloride/methanol (95:5) yielded the pure title compound, (3-Imidazol-1-yl-propyl)-{(1R,2R)-2-[4-(6-trifluoromethyl-benzo[b]thiophen-3-yl)-piperazin-1-ylmethyl]-cyclopropylmethyl}-amine as verified by NMR and LC/MS, yielding 36.2 mg, 76%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550469B2
Source datasetuspto-grants-2009_06
ORD IDord-5369a35d089e4a3e89af551359a821f7
Source noteuspto-grants-2009_06