(1S,2S)-1-{[5-(2,4-dichlorophenyl)-3,6-diethylpyrazin-2-yl]amino}-2,3-dihydro-1H-inden-2-ol → cis-(+/-)-4-{[3,6-Diethyl-5-(4-methoxy-2-methylphenyl)pyrazin-2-yl]amino}tetrahydrofuran-3-ol
反応式
ClC1C=C(Cl)C=CC=1C1N=C(CC)C(N[C@H]2C3C(=CC=CC=3)C[C@@H]2O)=NC=1CC.[N+](C1C=CC(C([O:39][C@H:40]2[C@@H:44]([NH:45][C:46]3[C:51]([CH2:52][CH3:53])=[N:50][C:49]([C:54]4[CH:59]=[CH:58][C:57]([O:60][CH3:61])=[CH:56][C:55]=4[CH3:62])=[C:48]([CH2:63][CH3:64])[N:47]=3)[CH2:43][O:42][CH2:41]2)=O)=CC=1)([O-])=O>>[CH2:52]([C:51]1[C:46]([NH:45][C@H:44]2[CH2:43][O:42][CH2:41][C@H:40]2[OH:39])=[N:47][C:48]([CH2:63][CH3:64])=[C:49]([C:54]2[CH:59]=[CH:58][C:57]([O:60][CH3:61])=[CH:56][C:55]=2[CH3:62])[N:50]=1)[CH3:53]参加物
3
反応物 2
生成物 1
実験手順
Following the procedure for the preparation of (1S,2S)-1-{[5-(2,4-dichlorophenyl)-3,6-diethylpyrazin-2-yl]amino}-2,3-dihydro-1H-inden-2-ol. but substituting cis-(+/−)-4-{[3,6-diethyl-5-(4-methoxy-2-methylphenyl)pyrazin-2-yl]amino}tetrahydrofuran-3-yl 4-nitrobenzoate and making non-critical variations provided the title compound as a colorless semi-solid. OAMS supporting ions at: ESI+ 358.2; MS (EI) m/z 357 (M+); HRMS (FAB) calcd for C20H27N3O3+H1 358.2130, found 358.2125.
出典と根拠
- ORDレコード
- ord-5b8c13943f2f43e5a37d2a38794f1226
- 出典データセット
- uspto-grants-2006_01
- 特許番号
- US06992087B2
反応ノート
読み込み中…