Thionyl Chloride → (Z)-(R)-4-amino-5-biphenyl-4-yl-2-methyl-pent-2-enoic acid hydrochloride
反応式
[C:1]1([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH:6]=[CH:5][C:4]([CH2:7][C@@H:8]([NH:15]C(OC(C)(C)C)=O)/[CH:9]=[C:10](/[CH3:14])\[C:11]([OH:13])=[O:12])=[CH:3][CH:2]=1.S(Cl)([Cl:31])=O>C(O)C>[ClH:31].[NH2:15][C@H:8]([CH2:7][C:4]1[CH:3]=[CH:2][C:1]([C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)=[CH:6][CH:5]=1)/[CH:9]=[C:10](/[CH3:14])\[C:11]([OH:13])=[O:12]参加物
反応条件
- 温度
- 65 °C
実験手順
5 g (Z)—(R)-5-Biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpent-2-enoic acid (5a, R1=Boc, R2=H, R3=CO2H) is added to ethanol (50 ml) at room temperature. The mixture was stirred for 15 min and a further quantity of ethanol (10 ml) added. The mixture is then heated to 65° C. Thionyl chloride (1.44 ml) is added and the mixture stirred for 30 min. The volatiles are removed under reduced pressure. Heptane (50 ml) is added to the residue and the volatiles removed under reduced pressure. Ethyl acetate (30 ml) is added to the residue. The solid is collected by filtration. A portion of the solid (1 g) is suspended in ethyl acetate and stirred for 1 h at room temperature. The solid is collected by filtration and dried in vacuo to afford (Z)—(R)-4-amino-5-biphenyl-4-yl-2-methyl-pent-2-enoic acid hydrochloride (5a, R1=H, R2=H, R3=CO2H). 1H-NMR (DMSO): 1.79 (3H), 2.88 (1H), 3.10 (1H), 4.79 (1H), 5.91 (1H), 7.24-7.60 (9H), 8.32 (3H), 12.90 (1H).
後処理
- stirringthe mixture stirred for 30 min
- customThe volatiles are removed under reduced pressure
- additionHeptane (50 ml) is added to the residue
- customthe volatiles removed under reduced pressure
- additionEthyl acetate (30 ml) is added to the residue
- filtrationThe solid is collected by filtration
- stirringstirred for 1 h at room temperature
- filtrationThe solid is collected by filtration
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-d1d3c7659a674f919d0a47b6a0e789e2
- 出典データセット
- uspto-grants-2015_07
- 特許番号
- US09085529B2
反応ノート
読み込み中…