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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599260Generated: October 30, 2026

Triethylamine → HCID 67063149, compound

https://huagongshe.com/reaction/599260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiphosgeneHCID 10426—
ReactantHCID 67063020HCID 67063020—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67063149HCID 6706314989%

Reaction Steps

To a solution of diphosgene (3.5 g, 17.7 mmol) in dioxane (350 mL) at 0° C. was slowly added a solution comprised of 5-((4-fluoro-3-nitrophenylamino)methyl)-N-methyl-2-(methylthio)pyrimidin-4-amine (5.2 g, 16.1 mmol) and Et3N (4.5 mL, 32.1 mmol) in dioxane (250 mL). The resultant reaction mixture was stirred at RT overnight. The solvent was removed in vacuo and the residue was partitioned between EtOAc and H2O. The combined organics were dried (Na2SO4) and concentrated to give crude product, which was washed with cold MeOH (5 mL) to give 3-(4-fluoro-3-nitrophenyl)-1-methyl-7-(methylthio)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one (5.0 g, 89% yield) as a brown solid. 1H NMR (300 MHz, DMSO-d6): δ 8.26 (s, 1 H), 8.20 (m, 1 H), 7.82 (m, 1 H), 7.64 (dd, J=6.9, 8.4 Hz, 1 H), 4.82 (s, 2 H), 3.29 (s, 3 H), 2.50 (s, 3 H); MS (ESI) m/z: 350.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897762B2
Source datasetuspto-grants-2011_03
ORD IDord-c2f02c6a5e4c488c84500c0b027e712b
Source noteuspto-grants-2011_03