تفاعل #477297

ord-99cbd25087a446b68f188c8b7bfd9dca

معادلة التفاعل

C=CCCCCN(C)C(=O)C1CC(O)CC1C(=O)NC1(C(=O)OCC)CC1C=C
diene
C=CCCCCN(C)C(=O)C1CC(O)CC1C(=O)NC1(C(=O)OCC)CC1C=C
1-{[2-(Hex-5-enylmethylcarbamoyl)-4-hydroxycyclopentanecarbonyl]amino}-2-vinylcyclopropane carboxylic acid ethyl ester
CCN(C(C)C)C(C)C
DIPEA
CCOCCl
chloromethylethyl ether
C=CCCCCN(C)C(=O)C1CC(OCOCC)CC1C(=O)NC1(C(=O)OCC)CC1C=C
title compound
C=CCCCCN(C)C(=O)C1CC(OCOCC)CC1C(=O)NC1(C(=O)OCC)CC1C=C
1-{[4-Ethoxymethoxy-2-(hex-5-enyl-methyl-carbamoyl)-cyclopentanecarbonyl]-amino}-2-vinyl-cyclopropanecarboxylic acid ethyl ester

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزconcentrated by rotary evaporation
  2. 2
    أخرىpurified by column chromatography on silica gel (EtOAc/petroleum ether 1:1→1:0) which

الإجراء التجريبي

To a stirred solution of the diene 1c (7.94 g, 0.02 mol) in DCM and DIPEA (9.7 ml, 6 eq) at 0° C. (ice-bath) was added chloromethylethyl ether (2.79 g, 3 eq). The reaction mixture was stirred at room temperature overnight, concentrated by rotary evaporation and purified by column chromatography on silica gel (EtOAc/petroleum ether 1:1→1:0) which gave the pure title compound as slightly yellow syrup (6.67 g, 74%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08383584B2uspto-grants-2013_02