反応式
[CH2:1]1[CH:5]2[CH2:6][CH2:7][CH2:8][CH:4]2[CH2:3][NH:2]1.OP(O)(O)=O.[ClH:14]>O>[ClH:14].[CH2:3]1[C@@H:4]2[CH2:8][CH2:7][CH2:6][C@@H:5]2[CH:1]=[N:2]1参加物
実験手順
To a 3-L 3-neck flask jacketed at 20° C. and stirred at 300 rpm was added 500 mL of dH2O and 20 mL of a 25 wt % octahydrocyclopenta[c]pyrrole solution in water. The pH was adjusted to approximately 7.6 with concentrated H3PO4 to give a colorless, homogeneous solution, to which 2.0 mL of A. niger catalase suspension (Novozyme; “Catalyzyme 101”) and 5.0 g of monoamine oxidase powder of the polypeptide of SEQ ID NO: 16 (prepared by the method of Example 3) were added to give a pale yellow solution. The head space of the vessel was swept with dry air at approximately 0.2 L/min. The pH of the reaction was maintained at 7.5 via feedback controlled addition of the 25 wt % octahydrocyclopenta[c]pyrrole solution in water in 20-100 μL portions. The dimer of (3aR,6aS) octahydrocyclopenta[c]pyrrole to precipitated from the reaction and the reaction mixture became a white slurry. After 380 mL of the 25 wt % octahydrocyclopenta[c]pyrrole solution in water had been added, the product was separated from the reaction mixture via steam distillation (still head temperature ˜98° C.). The receiver pot contained a suspension of the dimer of (3aS,6aR)-1,3a,4,5,6,6a-hexahydrocyclopenta[c]pyrrole in water. 1.1-1.2 equivalent of concentrated HCl was added to the receiver pot break the dimer and give a homogeneous solution of (3aS,6aR)-1,3a,4,5,6,6a-hexahydrocyclopenta[c]pyrrole hydrochloride in water. This solution was used directly to make (1S,3aR,6aS)-octahydrocyclopenta[c]pyrrole-1-carbonitrile in Example 27.
後処理
- customTo a 3-L 3-neck flask jacketed at 20° C.
- customto give a colorless, homogeneous solution
- additionwere added
- customto give a pale yellow solution
- customwith dry air at approximately 0.2 L/min
- temperatureThe pH of the reaction was maintained at 7.5 via feedback
- additionaddition of the 25 wt % octahydrocyclopenta[c]pyrrole solution in water in 20-100 μL portions
- customThe dimer of (3aR,6aS) octahydrocyclopenta[c]pyrrole to precipitated from the reaction
- additionAfter 380 mL of the 25 wt % octahydrocyclopenta[c]pyrrole solution in water had been added
- customthe product was separated from the reaction mixture via steam distillation (still head temperature ˜98° C.)
- additiona suspension of the dimer of (3aS,6aR)-1,3a,4,5,6,6a-hexahydrocyclopenta[c]pyrrole in water
出典と根拠
- ORDレコード
- ord-1aebc039240844cda70e239805278ea5
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08859784B2
関連ノート
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