Hydrochloric Acid → HCID 86692739, Verbindung

Temperatur

45 °C

To a solution of aqueous triethanolamine (684 mL, 100 mM) was added isopropylamine hydrochloride (102.6 g), pyridoxal phosphate (Vitamin B6; 1.14 g), and the enzyme ATA24 (22.8 g) [ATA-024 is also known as CDX-010 and purchased from Codexis, Inc., Redwood City, Calif., USA.] The mixture was treated with DMSO (228 mL) and heated to 45° C. using a Multimax (Mettler Toledo). The pH was adjusted to 8.6 when 4-benzyl-3-{[(1R,2R)-2-(4-bromophenyl)-4-oxocyclohexyl]carbonyl}-1,3-oxazolidin-2-one (5.7 g, 12.49 mmol) was added as a solution in DMSO (228 mL) by syringe pump over 3 h. An additional amount of the enzyme ATA24 (2 g) was added in 10 mL of buffer and allowed to react for approximately 4 h. An additional amount of the enzyme ATA24 (3 g) was added in 30 mL of buffer and the reaction aged overnight. The reaction was treated with aq. 6 N HCl to lower the pH to 2, and then aged for about 30 min. The reaction was then filtered and the enzyme precipitate was rinsed with 250 mL of 10% DMSO/pH 2.5 H2O (3×). The filtrate was extracted with MTBE (1 L), and the aqueous layer was separated, brought to pH 9.5 and subsequently extracted with MTBE (1 L). The organic layer was separated, washed with pH 11 brine (2×250 mL), dried (MgSO4), filtered and concentrated to afford the title compound.

1. additionAn additional amount of the enzyme ATA24 (2 g) was added in 10 mL of buffer and
2. customto react for approximately 4 h
3. additionAn additional amount of the enzyme ATA24 (3 g) was added in 30 mL of buffer and the reaction aged overnight
4. filtrationThe reaction was then filtered
5. washthe enzyme precipitate was rinsed with 250 mL of 10% DMSO/pH 2.5 H2O (3×)
6. extractionThe filtrate was extracted with MTBE (1 L)
7. customthe aqueous layer was separated
8. extractionsubsequently extracted with MTBE (1 L)
9. customThe organic layer was separated
10. washwashed with pH 11 brine (2×250 mL)
11. dry with materialdried (MgSO4)
12. filtrationfiltered
13. concentrationconcentrated

ORD-Eintrag

ord-72341aa5a549456693babaf22a268f15

Quelldatensatz

uspto-grants-2014_03

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08669252B2