反应 #40352

ord-98046a2630464160bd404d70de886952

反应方程式

CCN1c2cc3c(C(F)(F)F)cc(=O)[nH]c3cc2CCC1C
Compound 187
CCN1c2cc3c(C(F)(F)F)cc(=O)[nH]c3cc2CCC1C
4-Trifluoromethyl-7-methyl-6-ethyl-6,7,8,9-tetrahydropyrido[2,3-g]quinolin-2(1H)-one
CCOC(O)C(F)(F)F
trifluoroacetaldehyde ethyl hemiacetal
CC1CCc2cc3[nH]c(=O)cc(C(F)(F)F)c3cc2N1CC(F)(F)F
4-Trifluoromethyl-7-methyl-6-(2,2,2-trifluoroethyl)-6,7,8,9-tetrahydropyrido[2,3-g]quinolin-2(1H)-one

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他This compound was prepared in a similar fashion as

实验过程

This compound was prepared in a similar fashion as that described in Example 84 from Compound 187 (Structure 33 of Scheme VI, where R1=methyl, n=1) and trifluoroacetaldehyde ethyl hemiacetal. 1H NMR (400 MHz, CDCl3) 11.08 (br. s, 1H), 7.06 (s, 1H), 7.00 (s, 1H), 6.99 (s, 1H), 3.99 (m, 1H), 3.81 (m, 1H), 3.67 (m, 1H), 3.10-2.95 (m, 1H), 2.92-2.82 (m, 1H), 2.07-1.97 (m, 1H), 1.93-1.80 (m, 1H), 1.19 (d, 3H, J=6.5).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07727980B2uspto-grants-2010_06