Formate → (3R,4S)-3-(benzyloxy)tetrahydro-2H-pyran-4-amine

HRID 1183820

반응식

HRID 1183820 반응식
[NH2:1][C@H:2]([C:4]([OH:6])=O)[CH3:3].C([O-])=O.[Na+].OP([O-])([O-])=O.[Na+].[Na+].C1N=C(N)C2N=CN([C@@H:27]3[O:31][C@H:30](COP(OP(OC[C@H]4O[C@@H](N5C=C(C(N)=O)CC=C5)[C@H](O)[C@@H]4O)(O)=O)(O)=O)[C@@H](O)[C@H]3O)C=2N=1.[CH3:62][C:63]1[C:68](O)=[C:67]([CH:70]=O)[C:66]([CH2:72]OP(O)(O)=O)=CN=1.C([O-])=O.C(O[C@@H]1C(=O)CCOC1)C1C=CC=CC=1.Cl.C(=O)([O-])[O-].[K+].[K+]>O.C(OCC)(=O)C>[CH2:70]([O:6][C@@H:4]1[C@@H:2]([NH2:1])[CH2:3][CH2:27][O:31][CH2:30]1)[C:67]1[CH:68]=[CH:63][CH:62]=[CH:72][CH:66]=1

참가 물질

12

반응물 9

HCID 283FormateHCID 313Hydrochloric AcidHCID 1051Pyridoxal 5'-phosphateHCID 5950L-AlanineHCID 11430Potassium CarbonateHCID 24203Sodium Phosphate, DibasicHCID 439153NadhHCID 2723810Sodium FormateHCID 60209906(3S)-3-(benzyloxy)tetrahydro-4H-pyran-4-one

생성물 1

HCID 60209907(3R,4S)-3-(benzyloxy)tetrahydro-2H-pyran-4-amine

시약·촉매·용매 2

HCID 962Water용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of L-Alanine (200 g, 2.24 mol), sodium formate (76.0 g, 1.12 mmol), and sodium phosphate dibasic (28.7 g, 202 mmol) in 2.25 L of water adjusted to pH 7.5 was added NAD (2.2 g, 3.21 mmol), pyridoxal-5-phosphate (2.2 g, 8.90 mmol), lactase dehydrogenase-LDH (0.45 g, 0.22 mol), formate dehydrogenase-FDH (4.5 g, 0.20 mol), and TA P1G5 (4.5 g, 0.22 mol) [CDX TA P1G5=Codex Transaminase panel enzyme P1G5, which is commercially available from Codexis (Redwood City, Calif., USA)]. After all the components were completely dissolved, (3S)-3-(benzyloxy)tetrahydro-4H-pyran-4-one (45 g, 0.22 mol) was added and the pH was adjusted to pH 7.25 with 6 N HCl and aged at 30° C. After 15 h, potassium carbonate (700 g, 5.06 mol) was added slowly, followed by ethyl acetate (2.2 L). The mixture was filtered through a bed of Solka Floc and the cake was washed with ethyl acetate (250 mL). The combined filtrates were separated and the aqueous layer was extracted a second time with ethyl acetate (2 L). The combined organic extracts were concentrated in vacuo to provide crude (3R,4S)-3-(benzyloxy)tetrahydro-2H-pyran-4-amine.

후처리

  1. dissolutionAfter all the components were completely dissolved
  2. customaged at 30° C
  3. filtrationThe mixture was filtered through a bed of Solka Floc
  4. washthe cake was washed with ethyl acetate (250 mL)
  5. customThe combined filtrates were separated
  6. extractionthe aqueous layer was extracted a second time with ethyl acetate (2 L)
  7. concentrationThe combined organic extracts were concentrated in vacuo

출처 및 근거

ORD 기록
ord-8d291c3709a64264a924704d614ea267
출처 데이터셋
uspto-grants-2014_03
특허 번호
US08664387B2

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