反应 #40356

ord-1bab2121c57e480fb6fea7acf1aeed55

反应方程式

CCN1CCCc2cc3[nH]c(=O)cc(C(F)(F)F)c3cc21
Compound 192
CCN1CCCc2cc3[nH]c(=O)cc(C(F)(F)F)c3cc21
4-Trifluoromethyl-6-ethyl-6,7,8,9-tetrahydropyrido[2,3-g]quinolin-2(1H)-one
O=CC1CC1
cyclopropanecarboxaldehyde
O=c1cc(C(F)(F)F)c2cc3c(cc2[nH]1)CCCN3CC1CC1
4-Trifluoromethyl-6-cyclopropylmethyl-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 192 (Structure 33 of Scheme VI, where R1═H, n=1) and cyclopropanecarboxaldehyde. 1H NMR (400 MHz, CDCl3) 11.44 (br. s, 1H), 7.06 (s, 1H), 7.00 (s, 1H), 6.92 (s, 1H), 3.40 (t, 2H, J=5.6), 3.21 (d, 2H, J=6.2), 2.90 (t, 2H, J=6.3), 1.99 (m, 2H), 1.07 (m, 1H), 0.58 (m, 2H), 0.27 (m, 2H).

来源

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