1,1-Dimethylethyl N-[(1R)-2-[5-bromo-3-[[2-fluoro-6-(trifluoromethyl)phenyl]methyl]-3,6-dihydro-4-methyl-2,6-dioxo-1(2H)-pyrimidinyl]-1-phenylethyl]carbamate → 5-bromo-1-[2-fluoro-6-(trifluoromethyl)benzyl]-6-methyl-3-[2(R)-amino-2-phenylethyl]-pyrimidine-2,4(1H,3H)-dione
反応式
[Br:1][C:2]1[C:3](=[O:38])[N:4]([CH2:22][C@H:23]([NH:30]C(OC(C)(C)C)=O)[C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[C:5](=[O:21])[N:6]([CH2:9][C:10]2[C:15]([C:16]([F:19])([F:18])[F:17])=[CH:14][CH:13]=[CH:12][C:11]=2[F:20])[C:7]=1[CH3:8]>C(Cl)Cl.C(O)(C(F)(F)F)=O>[Br:1][C:2]1[C:3](=[O:38])[N:4]([CH2:22][C@H:23]([NH2:30])[C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[C:5](=[O:21])[N:6]([CH2:9][C:10]2[C:15]([C:16]([F:19])([F:18])[F:17])=[CH:14][CH:13]=[CH:12][C:11]=2[F:20])[C:7]=1[CH3:8]参加物
3
反応物 1
生成物 1
試薬・触媒・溶媒 1
実験手順
5-Bromo-1-[2-fluoro-6-(trifluoromethyl)benzyl]-6-methyl-3-[2(R)-tert-butoxycarbonylamino-2-phenylethyl]-pyrimidine-2,4(1H,3H)-dione 1e was dissolved in 20 mL/20 mL CH2Cl2/TFA. The resulting yellow solution was stirred at room temperature for 2 hours. The volatiles were evaporated and the residue was partitioned between EtOAc/sat. NaHCO3. The organic phase was dried over Na2SO4. Evaporation gave 2a as a yellow oil.
後処理
- customThe volatiles were evaporated
- customthe residue was partitioned between EtOAc/
- dry with materialThe organic phase was dried over Na2SO4
- customEvaporation
出典と根拠
- ORDレコード
- ord-64db694cfe6e43d993e785cea4b42409
- 出典データセット
- uspto-grants-2006_06
- 特許番号
- US07056927B2
反応ノート
読み込み中…