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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373608Generated: October 29, 2026

Sodium borohydride → HCID 57444325, compound

https://huagongshe.com/reaction/2373608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantN-(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]acetyl}phenyl)acetamideHCID 57444326—
SolventDichloromethaneHCID 6344—
ProductHCID 57444325HCID 5744432542%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (0.015 g, 1.6 eq) was added to a stirred solution of N-(3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]acetyl}phenyl)acetamide (0.102 g, 1 eq) in dry DCM (2 mL) cooled to 0° C. under an inert atmosphere. The reaction was warmed to room temperature and stirred for 18 hours. The mixture was diluted with DCM (10 mL) and washed with water (2×10 mL). The organic phase was dried over sodium sulfate and the solvent was removed under reduced pressure. The crude material was purified on SPE cartridge (Silica) using as eluant DCM-methanol (97:3), affording the title compound in 42% yield (0.104 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459456B2
Source datasetuspto-grants-2008_12
ORD IDord-2abe89e302444fb7a6cce5a4f8aa799e
Source noteuspto-grants-2008_12