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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726540Generated: October 31, 2026

Ethyl 3-benzyloxy-9-methyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxylate → 3-Benzyloxy-9-methyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxylic acid

https://huagongshe.com/reaction/1726540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-benzyloxy-9-methyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxylateHCID 21069953—
SolventEthyl acetate hexaneHCID 21226206—
Product3-Benzyloxy-9-methyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxylic acidHCID 2106986096%

Reaction Steps

Saponification of intermediate 14, ethyl 3-benzyloxy-9-methyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxylate, (0.225 g, 0.65 mmol) as described in the preparation of intermediate 7 gave 0.198 g (96% yield) of the title acid as white crystals; mp 167-168° C. (ethyl acetate-hexane). 1HNMR 400 MHz (CDCl3) δ ppm: 1.68 (3H, d, J=6.6 Hz, CH3), 3.93 (2H, m, CH2), 4.12-4.21 (1H, m, CH), 4.27-4.35 (1H, m, CH), 4.70 (1H, q, J=6.6 Hz, OCH), 5.53 (2H, ABq, JAB=11.1 Hz, OCH2), 7.39 (3H, m, aromatics), 7.55 (2H, m, aromatics). MS (ESI+) m/z 317 [M+H+]. Anal. Calcd for C1-6H16N2O5: C, 60.75; H, 5.10; N, 8.86. Found: C, 60.65; H, 5.05; N, 8.72.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491819B1
Source datasetuspto-grants-2009_02
ORD IDord-603393d012674d83a68ec808a5a277b4
Source noteuspto-grants-2009_02