Reacción #562670

Ecuación de reacción

Nicotinamide Adenine Dinucleotide

Pyridoxal-5-phosphate

Lactate

Formate

Sodium phosphate

sodium formate

D-Alanine

HCl

→

crude title compound

Rendimiento 80.0%

Propyl ([7R]-7-amino-6,7,8,9-tetrahydropyrido[1,2-α]indol-10-yl)acetate

Rendimiento 80.0%

Disolventes

water

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.DISSOLUTIONslowly dissolved
2. 2
   OtroThe flask was flushed with nitrogen and propyl (7-oxo-6,7,8,9-tetrahydropyrido[1,2-α]indol-10-yl)acetate from Step 5
3. 3
   workup.ADDITIONwas added as a DMSO (0.06 M) solution
4. 4
   workup.WAITaged at 30° C. overnight under nitrogen atmosphere
5. 5
   OtroUpon completion of the reaction
6. 6
   workup.ADDITIONwas added
7. 7
   workup.STIRRINGAfter stirring for 1 hr the reaction
8. 8
   Filtraciónwas filtered through a Celite bed
9. 9
   Lavadothe filter cake was washed twice with 0.1 N HCl
10. 10
    ExtracciónThe combined aqueous filtrate was extracted with 1 volume of MTBE
11. 11
    workup.ADDITIONThe aqueous layer was diluted with an equal volume of MTBE
12. 12
    OtroThe two phases were separated
13. 13
    Extracciónthe aqueous layer was extracted with MTBE
14. 14
    LavadoThe combined organic layers were washed with dilute sodium carbonate
15. 15
    Secadodried over Na2SO4
16. 16
    OtroEvaporation of the volatiles

Procedimiento

Sodium phosphate, dibasic (3.8 equiv.) and sodium formate (266 equiv.) were added to a solution of D-Alanine (38 equiv.) in water. The pH was measured as 7.6. Nicotinamide Adenine Dinucleotide (0.04 equiv.), Pyridoxal-5-phosphate (0.11 equiv.), Lactate dehydrogenase (1 equiv.), Formate dehydrogenase (1 equiv.), and Amine-Transaminase-117 (1 equiv.) were added under stirring and slowly dissolved. The measured pH was 7.3. The mixture was aged at 22° C. for 1 h. The flask was flushed with nitrogen and propyl (7-oxo-6,7,8,9-tetrahydropyrido[1,2-α]indol-10-yl)acetate from Step 5 was added as a DMSO (0.06 M) solution. The reaction was adjusted to pH 7.2 and aged at 30° C. overnight under nitrogen atmosphere. Upon completion of the reaction as determined by HPLC, the pH of the reaction was adjusted to pH 4.0 with 6 N HCl and Celite (20 g per L) was added. After stirring for 1 hr the reaction was filtered through a Celite bed and the filter cake was washed twice with 0.1 N HCl. The combined aqueous filtrate was extracted with 1 volume of MTBE. The organic layer did not contain amine and was discarded. The aqueous layer was diluted with an equal volume of MTBE and the pH of the mixture was adjusted to pH 9.5 using 5N NaOH. The two phases were separated and the aqueous layer was extracted with MTBE. The spent aqueous layer had no detectable amine and was discarded. The combined organic layers were washed with dilute sodium carbonate and dried over Na2SO4. Evaporation of the volatiles afforded the crude title compound (80%). The ee was determined as 99% by SFC assay. The SFC conditions are ADH column (250×4.6 mm, 5 um), isocratic 20% MeOH, 25 mM iso-proply amine/CO2, 2 ml/min, 35° C., 200 bar, 215 nm, 15 min. Under these conditions the desired R-amine has an 8.99 min retention time (S-amine; 5.82 min)

Fuente