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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372348Generated: November 1, 2026

Maleic Anhydride → HCID 54708351, compound

https://huagongshe.com/reaction/1372348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AnhydrideHCID 7923—
ReactantHCID 21069982HCID 21069982—
SolventAcetic AcidHCID 176—
ProductHCID 54708351HCID 5470835127%

Reaction Steps

To a solution of N-(2-aminobenzyl)-3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxamide (0 050 g, 0.114 mmol) in acetic acid (1.5 mL) was added maleic anhydride (0.013 g, 0.131 mmol) and the reaction mixture stirred in a sealed tube at 115 C for 18 h. Acetic acid was evaporated in vacuo and the residue was purified by preparative HPLC (YMC-Pack C-18) to afford the title compound (0.013 g, 27% yield): 1H NMR (400 MHz, CDCl3) δ ppm: 8.03 (1H, broad t), 7.59 (1H, m), 7.48 (2H, m), 7.19 (1H, m), 6.92 (2H, s), 4.48 (2H, d, J=6.1 Hz), 4.04 (4H, s), 1.62 (6H, s); HRMS calcd for C21H21N4O6: 425.1461. found 425.1451.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157447B2
Source datasetuspto-grants-2007_01
ORD IDord-7aba93c986b74a9d9565742129d44ce6
Source noteuspto-grants-2007_01