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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586442Generated: October 31, 2026

Water → HCID 9885921, compound

https://huagongshe.com/reaction/586442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22335522HCID 22335522—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9885921HCID 988592154%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of (±)-(E)-N-[4-[1-(1H-imidazol-1-yl)-2-methylpropyl]phenyl]-2-[(4-nitrophenyl)-methylene]propanamide (0.00742 mol) in THF (80 ml) and TiCl3 (30 ml) was stirred at 0° C. for 15 minutes. The mixture was poured into water, ice and NaOH 3N and extracted with CH2Cl2 (2×100 ml). The combined organic layers were dried, filtered and the solvent evaporated. The residue was taken up in CH2Cl2 and (C2H5)2O. The precipitate was filtered off and stirred K2CO3 10% and CH2Cl2, dried, filtered off and evaporated. The residue was crystallized from 2-propanone. The precipitate was filtered off, taken up in Na2CO3 10% and CH2Cl2. The organic layer was dried, filtered off and evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 96/4/0.1). The pure fractions were collected and evaporated. The residue was crystallized from (C2H5)2O, yielding 1.5 g (±)-(E)-2-[(4-aminophenyl)methylene]-N-[4-[1-(1H-imidazol-1-yl)-2-methylpropyl]phenyl]propanamide (compound 61 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936626B2
Source datasetuspto-grants-2005_08
ORD IDord-f4ea1d924f96482e86aff61314f47b06
Source noteuspto-grants-2005_08