Trifluoroacetic acid → (R)-tetrahydro-furan-2-carboxylic acid (2-amino-thiazol-4-ylmethyl)-methyl-amide
反応式
C(OC(=O)[NH:7][C:8]1[S:9][CH:10]=[C:11]([CH2:13][N:14]([CH3:22])[C:15]([C@H:17]2[CH2:21][CH2:20][CH2:19][O:18]2)=[O:16])[N:12]=1)(C)(C)C.C(O)(C(F)(F)F)=O>>[NH2:7][C:8]1[S:9][CH:10]=[C:11]([CH2:13][N:14]([CH3:22])[C:15]([C@H:17]2[CH2:21][CH2:20][CH2:19][O:18]2)=[O:16])[N:12]=1参加物
3
実験手順
The product from Step 1 was treated with TFA to cleave the BOC group (Method 1) to afford (R)-tetrahydro-furan-2-carboxylic acid (2-amino-thiazol-4-ylmethyl)-methyl-amide.
出典と根拠
- ORDレコード
- ord-bb597e1ad90f430a8deee0472d118142
- 出典データセット
- uspto-grants-2012_04
- 特許番号
- US08148380B2
反応ノート
読み込み中…