反応 #1994305

ord-617c81492f5345bb8e238069346866ac

反応方程式

CCOC(=O)/C(N)=C/C(=O)/C=C/c1ccc(Cl)cc1
(2Z,5E)-2-amino-6-(4-chlorophenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester
CCOC(=O)/C(N)=C/C(=O)/C=C/c1ccc(Cl)cc1
(2Z,5E)-2-Amino-6-(4-chlorophenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester
CCOC(=O)C1=CC(=O)CC(c2ccc(Cl)cc2)N1
6-(4-Chlorophenyl)-4-oxo-1,4,5,6-tetrahydropyridine-2-carboxylic acid ethyl ester

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他gave
  2. 2
    その他purification by silica gel chromatography
  3. 3
    洗浄eluting with 40% EtOAc/hexanes, 6-(4-chlorophenyl)-4-oxo-1,4,5,6-tetrahydropyridine-2-carboxylic acid ethyl ester (12; 25 g, 49%, 99% pure by HPLC) as an off-white solid

実験手順

Using the procedure of Example 5, (2Z,5E)-2-amino-6-(4-chlorophenyl)-4-oxo-hexa-2,5-dienoic acid ethyl ester (8; 47 g, 0.168 mol) in 1,4-dioxane (470 mL) in a 2 liter Parr reactor gave, following purification by silica gel chromatography eluting with 40% EtOAc/hexanes, 6-(4-chlorophenyl)-4-oxo-1,4,5,6-tetrahydropyridine-2-carboxylic acid ethyl ester (12; 25 g, 49%, 99% pure by HPLC) as an off-white solid: mp 93-94° C.; 1H NMR (400 MHz, CDCl3) δ 7.36 (q, J=8.6 Hz, 4H), 5.82 (s, 1H), 5.72 (br s, 1H), 4.74 (dd, J=14.2, 5.0 Hz, 1H), 4.35 (q, J=7.1 Hz, 2H), 2.68 (dd, J=16.3, 14.2 Hz, 1H), 2.58 (dd, J=16.4, 5.0 Hz, 1H), 1.36 (t, J=7.1 Hz, 3H); HRMS-ESI (m/z): calcd for C14H14ClNO3, 279.067. found, 279.066.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08598086B2uspto-grants-2013_12