HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037504Generated: October 31, 2026
HCID 59532380, compound → HCID 59532367, compound
https://huagongshe.com/reaction/2037504
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 59532380 | HCID 59532380 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59532367 | HCID 59532367 | 40% |
Reaction Steps
A solution of 2-((S)-3-((S)-1-(4′-fluorobiphenyl-4-yl)ethyl)-2-oxo-6-(thiophen-2-yl)-1,3-oxazinan-6-yl)acetic acid (218 mg, 0.5 mmol) in THF anhydrous (10 mL) was added BH3 (3.0 mL) at 0□ and then stirred at reflux for 2 h. Then the reaction mixture quenched by water and separated, extracted with EtOAc twice. The organic phases was dried over Na2SO4, filtered and concentrated to afford the residue, which was purified by TLC to give (S)-3-((S)-1-(4′-fluorobiphenyl-4-yl)ethyl)-6-(2-hydroxyethyl)-6-(thiophen-2-yl)-1,3-oxazinan-2-one (85 mg, 40%). LC-MS Method 3 tR=1.35, min, m/z=426, 448; 1H NMR (CD3OD): 1.50 (m, 3H), 2.15 (m, 2H), 2.30 (m, 1H), 2.40 (m, 1H), 2.60 (m, 1H), 3.15 (m, 1H), 3.45 (m, 1H), 3.70 (m, 1H), 5.60 (m, 1H), 6.90 (m, 1H), 7.00 (m, 1H), 7.10 (m, 4H), 7.35 (m, 3H), 7.55 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575156B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-234feea8f9e04bb7a559225ef3c9d2c3 |
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| Source note | uspto-grants-2013_11 |
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