تفاعل #2208137

ord-320da35254c74644aaf8c85e6628f12e

معادلة التفاعل

O=C(OCc1ccccc1)N1CCC2(CC1)CO2
benzyl 1-oxa-6-aza-spiro[2.5]octane-6-carboxylate
O=C1CCCCN1
piperidone
C=S(C)(C)=O
dimethylsulfoxonium methylide
N#Cc1ccc(N)cc1
4-aminobenzonitrile
N#Cc1ccc(NCC2(O)CCN(C(=O)OCc3ccccc3)CC2)cc1
title compound
N#Cc1ccc(NCC2(O)CCN(C(=O)OCc3ccccc3)CC2)cc1
Benzyl 4-((N-(4-cyanophenyl)amino)methyl)-4-hydroxypiperidine-1-carboxylate

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe excess of the aniline was removed by chromatography on silica gel with dichloromethane

الإجراء التجريبي

A mixture of 20.0 g (80.9 mmol) benzyl 1-oxa-6-aza-spiro[2.5]octane-6-carboxylate (prepared from the protected piperidone and dimethylsulfoxonium methylide according to J. Med. Chem. 1983, 26, 855; U.S. Pat. No. 4,353,901) and 47.0 g (397.8 mmol) 4-aminobenzonitrile were heated at 160° C. for 30 hours until no starting epoxide could be detected by TLC. It was cooled to room temperature, and the excess of the aniline was removed by chromatography on silica gel with dichloromethane. The title compound was obtained after enhancing the polarity of the eluent by addition of 5% ethanol.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06693109B2uspto-grants-2004_02