(1,2-Oxazol-5-yl)methanethiol → 4-[[(1R)-2-Hydroxy-1-methylethyl]amino]-2-[(5-isoxazolylmethyl)thio]-7(8H)-pteridinone
反応式
F[C:2]1[C:7](F)=CC=C[C:3]=1[CH2:9][S:10]([C:13]1[N:22]=[C:21]([NH:23][C@H:24]([CH3:27])[CH2:25][OH:26])[C:20]2[N:19]=[CH:18][C:17](=[O:28])[NH:16][C:15]=2[N:14]=1)(=O)=O.[O:29]1C(CS)=CC=[N:30]1>>[OH:26][CH2:25][C@H:24]([NH:23][C:21]1[C:20]2[N:19]=[CH:18][C:17](=[O:28])[NH:16][C:15]=2[N:14]=[C:13]([S:10][CH2:9][C:3]2[O:29][N:30]=[CH:7][CH:2]=2)[N:22]=1)[CH3:27]参加物
3
実験手順
The titled compound (0.038 g) was prepared by the method of Example 13, step (c) using the product from Example 13, step (a) (0.10 g) and 5-isoxazolylmethylmercaptan (0.057 g).
出典と根拠
- ORDレコード
- ord-1ce814bc3d9648249797053e4cdb2743
- 出典データセット
- uspto-grants-2005_04
- 特許番号
- US06875868B2
反応ノート
読み込み中…