Réaction #1509625

ord-eaeb27b421b949c1bbd9dd2c14e62d68

Équation de réaction

O=C(c1cc(Br)c(Br)[nH]1)C(Cl)(Cl)Cl
2,2,2-trichloro-1-(4,5-dibromo-1H-pyrrol-2-yl)-ethanone
CCCCCCCCCCCCNC(=O)CCCc1c[nH]c(N)n1.Cl
2-trichloroacetyl-1-methylpyrrole
CCCCCCCCCCCCNC(=O)CCCc1c[nH]c(N)n1.Cl
4-(2-amino-1H-imidazol-4-yl)-N-dodecyl-butyramide hydrochloride
Cn1c(C(=O)C(Cl)(Cl)Cl)cc(Br)c1Br
title compound 14
Rendement 96.0%
Cn1c(C(=O)C(Cl)(Cl)Cl)cc(Br)c1Br
2,2,2-trichloro-1-(4,5-dibromo-1-methyl-pyrrol-2-yl)-ethanone
Rendement 96.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

Using the same general procedure as used for the synthesis of 2,2,2-trichloro-1-(4,5-dibromo-1H-pyrrol-2-yl)-ethanone 8, 5.00 g of 2-trichloroacetyl-1-methylpyrrole 12 gave 8.14 g (96%) of the title compound 14 as white needles. 1H NMR (300 MHz, DMSO-d6) δ 7.60 (s, 1H), 3.96 (s, 3H); 13C NMR (100 MHz, DMSO-d6) δ 170.86, 123.81, 122.68, 120.58, 99.58, 94.89, 37.60; HRMS (FAB) calcd for C7H4Br2Cl3NO (M+) 380.7725, found 380.7744.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08927029B2uspto-grants-2015_01