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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390345Generated: October 29, 2026

Dimethylformamide → HCID 58458900, compound

https://huagongshe.com/reaction/390345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHydrazineHCID 9321—
ReactantOxalyl chlorideHCID 65578—
Reactant3-(Benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxylic acidHCID 21069858—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 58458900HCID 5845890027%

Reaction Steps

To a stirred suspension of 3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxylic acid (prepared according to the procedure in Naidu, B. N. et al WO2005118593) (0.66 g, 2 mmol) in CH2Cl2 (10 mL) containing catalytic DMF was added oxalyl chloride in CH2Cl2 (2 M, 2 mL, 4 mmol) at room temperature. After 3 h, the resulting clear reaction solution was concentrated to remove excess oxalyl chloride. The resulting residue was re-dissolved in CH2Cl2 (20 mL) and treated with anhydrous hydrazine (0.34 mL, 10 mmol). After 2 h at room temperature, the reaction mixture was concentrated and the residue was taken up in EtOAc (100 mL) and washed with sat. NaHCO3 (10 mL), water (10 mL), brine (10 mL) then dried (Na2SO4), filtered and concentrated to give a white solid. This was digested with Et2O (20 mL) and filtered. Concentration of filtrate provided the title compound (0.17 g, 27% yield). 1HNMR (500 MHz, CDCl3) δ: 8.35 (1H, s), 7.55 (2H, d, J=7.3 Hz), 7.38-7.31 (3H, m), 5.30 (2H, s), 4.03-3.97 (6H, m), 1.60 (6H, s). HRMS (M+H) calcd for C17H21N4O5: 345.1563. found: 345.1577.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383639B2
Source datasetuspto-grants-2013_02
ORD IDord-d4ab0a45e9d642b6b4f34ba2e67fc176
Source noteuspto-grants-2013_02