HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037565Generated: October 30, 2026
HCID 58109670, compound → HCID 58109698, compound
https://huagongshe.com/reaction/2037565
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 58109670 | HCID 58109670 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58109698 | HCID 58109698 | 25.9% |
Reaction Steps
To a solution of methyl 2-(4-((S)-1-((R)-6-(3-(4-methoxybenzyloxy)propyl)-2-oxo-6-phenyl-1,3-oxazinan-3-yl)ethyl)phenyl)acetate (100 mg, 0.188 mmol) in THF (2 mL) was added methylmagnesium bromide (0.3 mL, 3 mol/L) at −78° C. The formed mixture was stirred for 3 h. The reaction was quenched by aqueous solution of NH4Cl. The organic phase was separated and concentrated to provide the crude product, which was purified by TLC to give (R)-3-((S)-1-(4-(2-hydroxy-2-methylpropyl)phenyl)ethyl)-6-(3-hydroxypropyl)-6-phenyl-1,3-oxazinan-2-one (10 mg, 10%). 1H NMR (CDCl3): δ=1.08 (d, 6H), 1.19 (m, 2H), 1.42 (d, 3H), 1.64 (m, 2H), 1.84 (m, 2H), 2.04-2.19 (m, 4H), 2.53 (s, 2H), 2.80 (m, 1H), 3.29 (t, 2H), 3.72 (s, 3H), 4.25 (s, 2H), 5.54 (q, 1H), 6.74 (m, 5H), 6.82 (m, 2H), 7.10 (m, 3H), 7.23 (m, 4H).
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-ceba5c850e4146f99b44554277104c3e |
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| Source note | uspto-grants-2013_11 |
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