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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726652Generated: October 30, 2026

Acetyl chloride → HCID 58777387, compound

https://huagongshe.com/reaction/1726652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant(R)-N-(4-Fluoro-2-(2-(hydroxymethyl)-5-oxopyrrolidin-1-yl)benzyl)-3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxamideHCID 58777341—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58777387HCID 5877738767%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of intermediate 192, (R)—N-(4-fluoro-2-(2-(hydroxymethyl)-5-oxopyrrolidin-1-yl)benzyl)-3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxamide (0.045 g, 0.082 mmol) in tetrahydrofuran (5 mL) was added acetyl chloride (12.8 μL, 0.180 mmol) and diisopropylethylamine (31.4 μL, 0.180 mmol). The reaction mixture was stirred at 23° C. for 4 h. NaHCO3 (1N in H2O, 30 mL) was then added and the organic material was extracted with ethyl acetate (2×25 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo. The residue was purified on a Biotage system using a silica gel column with ethyl acetate/Hexanes (1:1) to ethyl acetate 100% as eluent to afford the title compound (0.032 g, 67% yield): 1HNMR 400 MHz (MeOD) δ ppm: 7.48 (3H, m), 7.33 (3H, m), 7.16 (1H, m), 7.03 (1H, m), 5.24 (2H, s), 4.60 (1H, m), 4.55 (1H, m), 4.22 (1H, dd, J=12.0, 4.5 Hz), 4.08 (2H, t, J=5.0 Hz), 3.99 (3H, m), 2.62 (2H, m), 2.44 (1H, m), 2.09-1.92 (5H, m), 1.62 (3H, s), 1.61 (3H, s). LCMS (M+H)+ m/z 593.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491819B1
Source datasetuspto-grants-2009_02
ORD IDord-c2e8831efc944776803280480a0f6d04
Source noteuspto-grants-2009_02