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HRID1861276

反应详情

EQUATION

反应方程式

HRID 1861276 的结构方程式

REACTANTS

反应物

2
结构：C=CCOC(=O)NC1CC(=O)OC1OC1CCCC1
HCID18465755

未命名化合物

结构：CC(NC(=O)c1ccc(N)c(Cl)c1)C(=O)N1CCCC1C(=O)NC1CC(=O)OC1OCCc1ccccc1
HCID22977512

未命名化合物

PRODUCTS

生成物

1
结构：CC(=O)Nc1ccc(C(=O)NC(C)C(=O)N2CCCC2C(=O)NC2CC(=O)OC2OC2CCCC2)cc1Cl
HCID22977477

未命名化合物

收率 69%

PROCEDURE

实验过程

Prepared from 97b and (2-cyclopentyloxy-5-oxo-tetrahydro-furan-3-yl)-carbamic acid allyl ester according to the procedure used to prepare 98a to afford 215 mg of title compound (69% yield). 1H-NMR (500 MHz, 1:1 CDCl3:CD3OD) δ 1.35-1.90 (m, 11H), 1.90-2.35 (m, 4H), 2.24 (s, 3H), 2.40-3.10 (m, 2H), 3.50-3.95 (m, 3H), 4.15-4.90 (m, 3H), 5.44 (s, 0.55H), 5.56 (s, 0.15H), 5.64 (d, 0.22H), 5.71 (d, 0.08H), 7.70-8.25 (m, 3H). Analytical HPLC: 12.13 min. LC-MS (ES+): m/e=549.2 (M+H+).