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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243166Generated: October 30, 2026

Methyl formate → HCID 11385587, compound

https://huagongshe.com/reaction/1243166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl formateHCID 7865—
ReactantHCID 11235766HCID 11235766—
ProductHCID 11385587HCID 11385587—

Reaction Steps

3-(4-Methoxy-phenyl)-7-phenylamino-1-piperidin-3-yl-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one (95 mg, 0.22 mmol) (from Example 4b supra) was dissolved at room temperature in methylformate (5 mL) (Aldrich). After stirring overnight the reaction mixture was concentrated to the crude product, which was purified by silica gel column chromatography with a 0–100% ethyl acetate in hexanes and then a 0–20% tetrahydrofuran in ethyl acetate gradient. After a precipitation out of dichloromethane with excess of pentane, 3-[3-(4-methoxy-phenyl)-2-oxo-7-phenylamino-3,4-dihydro-2H-pyrimido[4,5-d]pyrimidin-1-yl]-piperidine-1-carbaldehyde was isolated as an off-white solid. (Yield 90 mg, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115740B2
Source datasetuspto-grants-2006_10
ORD IDord-c0df0d85864f47c38dd7aae4a90f4c9e
Source noteuspto-grants-2006_10