反应 #1509632

ord-0d16de46efc94dcdb897229b10391d8d

反应方程式

Cl.Cl.NCCC=C1NC(N)=NC1=O
2-amino-5-(3-amino-propylidene)-1,5-dihydro-imidazol-4-one dihydrochloride
Cl.Cn1c(C(=O)NCCCc2c[nH]c(N)n2)cc(Br)c1Br
dihydrosventrin hydrochloride
Cl.Cn1c(C(=O)NCCCc2c[nH]c(N)n2)cc(Br)c1Br
4,5-dibromo-1-methyl-pyrrole-2-carboxylic acid [3-(2-amino-1H-imidazol-4-yl)-propyl]-amide hydrochloride
Cl.Cn1c(C(=O)NCCC=C2NC(N)=NC2=O)cc(Br)c1Br
title compound 32
收率 47.0%
Cl.Cn1c(C(=O)NCCC=C2NC(N)=NC2=O)cc(Br)c1Br
4,5-dibromo-1-methyl-pyrrole-2-carboxylic acid [3-(2-amino-5-oxo-3,5-dihydro-imidazol-4-ylidene)-propyl]-amide hydrochloride
收率 47.0%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Using the same general procedure as used for 2-amino-5-(3-amino-propylidene)-1,5-dihydro-imidazol-4-one dihydrochloride, 0.100 g of dihydrosventrin hydrochloride 23 gave 0.048 g (47%) of the title compound 32 as a tan solid ((Z)-isomer exclusively). 1H NMR (300 MHz, CD3OD) δ 6.84 (s, 1H), 6.16 (t, 1H, J=7.8 Hz), 3.91 (s, 3H), 3.46 (t, 2H, J=6.9 Hz), 2.59 (dt, 2H, J=6.9, 14.7 Hz); 13C NMR (100 MHz, DMSO-d6) δ 163.80, 163.00, 157.19, 130.63, 129.04, 119.42, 115.92, 112.67, 99.09, 39.06, 36.28, 28.73; HRMS (ESI) calcd for C12H14Br2N5O2 (MH+) 417.9509, found 417.9511.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08927029B2uspto-grants-2015_01