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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367549Generated: October 28, 2026

NADP nicotinamide-adenine-dinucleotide phosphate → HCID 59619444, compound

https://huagongshe.com/reaction/1367549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNADP nicotinamide-adenine-dinucleotide phosphateHCID 5886—
ReactantSodium HydroxideHCID 14798—
Reactant4-Morpholineethanesulfonic acidHCID 78165—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantMagnesium ChlorideHCID 5360315—
ReactantHCID 59619308HCID 59619308—
SolventEthyl AcetateHCID 8857—
ProductHCID 59619444HCID 5961944467.7%

Reaction Steps

A solution of (1R,2R)-4-oxo-cyclopentane-1,2-dicarboxylic acid monoethyl ester (example 1, step 1, 6.0 g) in an aqueous buffer (600 mL, 30 mM; 2-(N-morpholino)ethanesulfonic acid; 0.5 M D-glucose [10 equ.]; 2 mM Magnesium chloride) was adjusted to pH 6.4 at 35° C. Under stirring the reduction was started by the addition of the cofactor NADP (120 mg), the cofactor regeneration enzyme-glucose dehydrogenase (120 mg GDH 102 [Codexis]) and the reductase (1.2 g KRED-NADP-174 [Codexis]). During the 69 h reaction time at 35° C. the pH was kept at pH 6.5 by the addition of 1M NaOH. Afterwards the enzymes were denatured by adjusting to pH 2, adding a total of 300 mL ethyl acetate and a total of 60 g filter aid—Dicalite under stirring of at least 1.5 h. After filtration, two further extractions with 200 mL ethyl acetate, treatment of the combined organic phases with magnesium sulfate, evaporation and drying for 4 h on a high vacuum, 4.1 g of the title compound was isolated. MS: 201.07 (M−H)−; chiral GC: d.r.: 1.4:97.3:1.4: 0.0 [BGB-172 (BGB Analytik AG), 30 m*0.25 mm; 0.25 μm; H2; 2° C./min, 100° C. to 200° C.]. An additional extraction of the aqueous phase with further 200 mL ethyl acetate yielded after treatment with magnesium sulfate, evaporation and drying for 4 h on a high vacuum in 1.62 g of the title compound. MS: 201.07 (M−H)−; chiral GC: d.r.: 1.3:96.3:1.6:0.4. The summing up gave a total yield of 5.72 g (93.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893099B2
Source datasetuspto-grants-2011_02
ORD IDord-886a50ba29b2458eae5bd520ce8ecccd
Source noteuspto-grants-2011_02