1-(Thiazol-2-yl)piperazine → 1-(2,2,4,6,7-Pentamethyl-2,3-dihydro-1-benzofuran-5-yl)-4-(1,3-thiazol-2-yl)piperazine
反応式
Br[C:2]1[C:3]([CH3:15])=[C:4]([CH3:14])[C:5]2[O:9][C:8]([CH3:11])([CH3:10])[CH2:7][C:6]=2[C:12]=1[CH3:13].[S:16]1[CH:20]=[CH:19][N:18]=[C:17]1[N:21]1[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]1>>[CH3:10][C:8]1([CH3:11])[CH2:7][C:6]2[C:12]([CH3:13])=[C:2]([N:24]3[CH2:25][CH2:26][N:21]([C:17]4[S:16][CH:20]=[CH:19][N:18]=4)[CH2:22][CH2:23]3)[C:3]([CH3:15])=[C:4]([CH3:14])[C:5]=2[O:9]1参加物
3
実験手順
By using 5-bromo-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran (404 mg, 1.50 mmol) synthesized in Reference example 4 and 1-(1,3-thiazol-2-yl)piperazine (508 mg, 3.00 mmol), the reaction was carried out in the same manner as Example 21 to synthesis the title compound 196 mg (yield 36%). Melting point was 150 to 151° C. (hexane-ethyl acetate).
出典と根拠
- ORDレコード
- ord-c0ec5fdbf8f84449b7c6d87207590810
- 出典データセット
- uspto-grants-2015_02