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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264660Generated: November 1, 2026

Sodium Hydroxide → HCID 57060444, compound

https://huagongshe.com/reaction/264660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 57090662HCID 57090662—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57060444HCID 57060444—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 195 mg (0.325 mmol) of (2R*,4S*)-2-benzyl-1-(2,4-dichlorobenzoyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine and 26 mg (0.649 mmol) of sodium hydroxide in 2 ml of methanol and 2 ml of tetrahydrofuran is left to stir at 0° C. for 18 hours. The reaction mixture is then concentrated, taken up in methylene chloride and washed with water and brine. The organic phases are dried over magnesium sulfate and evaporated to dryness. The yellow oil is chromatographed on silica gel with methylene chloride/methanol/conc. ammonia (800:50:1). The title compound ##STR66## is obtained (157 mg, 96%) as white foam. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.45, FD-MS: M+ =503,505.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646144
Source datasetuspto-grants-1997_07
ORD IDord-17eaf6f7f92e4aaa8fe615cf9c08f76c
Source noteuspto-grants-1997_07