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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737025Generated: November 2, 2026

Sodium Hydroxide → HCID 57060444, compound

https://huagongshe.com/reaction/1737025

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 numberUS05541195
Source datasetuspto-grants-1996_07
ORD IDord-2a1352763906401fa5e2438fb84d20d0
Source noteuspto-grants-1996_07