Phenylalanine amide → (2R)-2-amino-3-phenylpropanamide
反応式
[NH2:1][C@H:2]([C:10]([NH2:12])=[O:11])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>O>[NH2:1][C@@H:2]([C:10]([NH2:12])=[O:11])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1参加物
3
実験手順
In accordance with the process described in JP Patent Application Laying Open (Kokai) No. 62-55097, Enterobacter cloacae N-7901 (FERM BP-873) was cultured. This culture solution, 500 mL, was centrifuged, and the wet cells were then suspended in distilled water to prepare a 1,140 g cell suspension. D, L-phenylalanine amide, 60 g, was dissolved in this suspension, and the mixture was then allowed to react at 40° C. for 24 hours. After the reaction, cells were removed by centrifugation and 1,150 g of an aqueous solution containing 2.5% by mass each of L-phenylalanine and D-phenylalanine amide was obtained.
後処理
- customto prepare a 1,140 g cell suspension
- customto react at 40° C. for 24 hours
- customAfter the reaction, cells
- customwere removed by centrifugation and 1,150 g of an aqueous solution
- additioncontaining 2.5% by mass each of L-phenylalanine
出典と根拠
- ORDレコード
- ord-48e42abb38bb4bc8ad7561b1cc61f9b2
- 出典データセット
- uspto-grants-2005_09
- 特許番号
- US06949658B2
反応ノート
読み込み中…