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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985095Generated: October 30, 2026

Ammonium Chloride → HCID 10215337, compound

https://huagongshe.com/reaction/985095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69586067HCID 69586067—
SolventMethanolHCID 887—
ProductHCID 10215337HCID 1021533778%

Reaction Steps

6.0 g of (8R,9R)-8-hydroxy-2-methoxymethyl-3-methyl-9-phenyl-7,8,9,10-tetrahydro-imidazo[1,2-h][1,7]naphthyridin-7-one are suspended in 40 ml methanol and 0.6 g sodium borohydride are added in small portions over a period of 30 min. After 1 h at ambient temperature the reaction mixture is poured onto of 60 ml icewater and 2 g ammonium chloride. The organic layer is separated and the aqueous phase extracted three times with dichloromethane. The combined organic phases are dried over anhydrous sodium sulfate and the solvent removed in vacuo. The residue is purified by column chromatography on silica gel (eluent: dichloromethane/methanol 100:1). Crystallization from diethyl ether yields 4.7 g (78%) of the title compound as a light brown solid (BYK237362, m.p. 102-104° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06869949B2
Source datasetuspto-grants-2005_03
ORD IDord-d4b57515bdaa4ebdad834c790a4f35d1
Source noteuspto-grants-2005_03