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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960013Generated: October 28, 2026

Water → {2-[n-(Cyclohexylmethyl)-n-ethylamino]-7-fluoroquinolin-3-yl}methanol

https://huagongshe.com/reaction/1960013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57861258HCID 57861258—
SolventEthanolHCID 702—
Product{2-[n-(Cyclohexylmethyl)-n-ethylamino]-7-fluoroquinolin-3-yl}methanolHCID 57861244—

Reaction Steps

To a mixture of 2-[N-(cyclohexylmethyl)-N-ethylamino]-7-fluoroquinoline-3-carbaldehyde (230 mg, 0.73 mmol) in ethanol (2 mL) is added sodium borohydride (30 mg, 0.79 mmol) and the mixture is stirred for 2 hours. After addition of sat. ammonium chloride and water, the mixture is extracted with ethyl acetate. The combined organic layer is washed with brine, dried over magnesium sulfate, filtered and concentrated to give [N-(cyclopentylmethyl)-N-ethylamino]quinolin-3-yl}methanol, which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410275B2
Source datasetuspto-grants-2013_04
ORD IDord-5eec75b9b8044723b15daa36284ad340
Source noteuspto-grants-2013_04