HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605463Generated: October 30, 2026
NADP nicotinamide-adenine-dinucleotide phosphate → 1,1-Dimethylethyl N-[(1S,2R)-3-chloro-2-hydroxy-1-(phenylmethyl)propyl]carbamate
https://huagongshe.com/reaction/605463
Participants
| Role | Name | HCID | Charge |
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| Reactant | NADP nicotinamide-adenine-dinucleotide phosphate | HCID 5886 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | tert-butyl N-((2S)-4-chloro-3-oxo-1-phenylbutan-2-yl)carbamate | HCID 9926241 | — |
| Product | 1,1-Dimethylethyl N-[(1S,2R)-3-chloro-2-hydroxy-1-(phenylmethyl)propyl]carbamate | HCID 9944139 | 99% |
Reaction Steps
Glucose dehydrogenase (manufactured by Amano Enzyme) 1250 U, glucose 3 g, NADP 4 mg, (3S)-1-chloro-3-tert-butoxycarbonylamino-4-phenyl-2-butanone 0.25 g were added to 22.5 ml of a cell-free extract of E. coli HB101 (pNTOM4) prepared in Example 7, and the mixture was is stirred at 30° C. while adjusting to pH 6.5 by dropwise addition of 5 M sodium hydroxide. (3S)-1-chloro-3-tert-butoxycarbonylamino-4-phenyl-2-butanone (0.25 g) was added at 2 hr, 4 hr and 6 hr from the start of the reaction and 1.25 g thereof was added at 8 hr from the start of the reaction, and the mixture was reacted for 31 hr. After completion of the reaction, the reaction mixture was extracted with toluene, desolvated and the extract was analyzed in the same manner as in Example 8. As a result, (2R,3S)-1-chloro-3-tert-butoxycarbonylamino-4-phenyl-2-butanol (yield 99.0%, diastereomeric excess 99.8% d.e.) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915022B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-f68660f9872741859f132ce87fdcb4e5 |
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| Source note | uspto-grants-2011_03 |
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