Tetrahydrofuran → HCID 69735894、化合物

反応式

C(O[C:4](=O)[CH:5]([C:16]1[C:21]([NH:22][C:23]([O:25][CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[O:24])=[CH:20][CH:19]=[C:18]([O:33][CH3:34])[N:17]=1)S(C1C=CC(C)=CC=1)(=O)=O)C.[CH3:36][C:37](C)([O-:39])C.[K+].C1C[O:45][CH2:44]C1>>[CH2:37]([O:39][C:44](=[O:45])[CH:4]=[CH:5][C:16]1[C:21]([NH:22][C:23]([O:25][CH2:26][C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=2)=[O:24])=[CH:20][CH:19]=[C:18]([O:33][CH3:34])[N:17]=1)[CH3:36]

参加物

反応物 3

HCID 8028Tetrahydrofuran2 回

HCID 23665647Potassium tert-butoxide

HCID 69736562HCID 69736562、化合物

生成物 1

HCID 69735894HCID 69735894、化合物

実験手順

To a cooled (5° C.) solution of 15.7 g (0.031 mol) of (3-benzyloxycarbonylamino-6-methoxy-pyridin-2-yl)-(toluene-4-sulfonyl)-acetic acid ethyl ester dissolved in 160 mL of THF is added, dropwise, 31 mL of a 1N solution of potassium-t-butoxide dissolved in THF. The reaction mixture is warmed to room temperature and stirred for 2 hours. The reaction is quenched with 5 mL of water and evaporated. The residue is dissolved in 200 mL of ethyl acetate and 200 mL of water. The ethyl acetate layers are dried (Na2SO4) and evaporated. The residue is chromatographed on 375 grams of silica gel using 7/3 hexanes/ethyl acetate as the eluant. Appropriate fractions are combined and evaporated to yield 5.57 grams of 3-[3-benzyloxycarbonylamino-6-methoxy-pyridin-2-yl]-acrylic acid ethyl ester. 1H NMR (CDCl3) δ7.8 (m, 2H), 7.4 (m, 2H), 7.0 (m, 1H), 6.8 (m, 1H), 6.7 (m, 1H), 5.2 (s, 2H), 4.2 (q, 2H) 3.9 (s, 3H), 1.3 (t, 3H). Mass spectrum: m/e=357 (p+1).