反応式
C(OC(C1NN=C(COC2C=CC=CC=2)C=1)=O)C.CC1(C)OC[C@H](CO)N1C(OC(C)(C)C)=O.[C:35]([O:39][C:40]([N:42]1[C@H:46]([CH2:47][N:48]2[C:52]([C:53]([O:55][CH2:56][CH3:57])=[O:54])=[CH:51][C:50]([CH2:58][O:59][C:60]3[CH:65]=[CH:64][CH:63]=[CH:62][CH:61]=3)=[N:49]2)[CH2:45][O:44][C:43]1([CH3:67])[CH3:66])=[O:41])([CH3:38])([CH3:37])[CH3:36]>>[C:35]([O:39][C:40]([N:42]1[C@@H:46]([CH2:47][N:48]2[C:52]([C:53]([O:55][CH2:56][CH3:57])=[O:54])=[CH:51][C:50]([CH2:58][O:59][C:60]3[CH:61]=[CH:62][CH:63]=[CH:64][CH:65]=3)=[N:49]2)[CH2:45][O:44][C:43]1([CH3:66])[CH3:67])=[O:41])([CH3:36])([CH3:37])[CH3:38]参加物
4
実験手順
The compound was prepared from 5-phenoxymethyl-2H-pyrazole-3-carboxylic acid ethyl ester and (S)-1-boc-2,2-dimethyl-4-hydroxymethyl-oxazolidine using the method described in the preceding example 29 (R)-4-(5-ethoxycarbonyl-3-phenoxymethyl-pyrazol-1-ylmethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester.
出典と根拠
- ORDレコード
- ord-e1cfb0ccc921469891d6216e972cffe1
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08592422B2
関連ノート
読み込み中…