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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946792Generated: November 2, 2026

Carbonate Ion → HCID 67529207, compound

https://huagongshe.com/reaction/1946792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonate IonHCID 19660—
ReactantTriacetoxyborohydrideHCID 2724942—
Reactanttert-Butyl alaninate--hydrogen chloride (1/1)HCID 21916431—
ReactantHCID 59446872HCID 59446872—
SolventDichloromethaneHCID 6344—
ProductHCID 67529207HCID 67529207—

Reaction Steps

A solution of 6-((cyclopropylmethyl)(propyl)amino)-N-(4-formyl-2-methylphenyl)pyrimidine-4-carboxamide (Intermediate 29, 100 mg; 0.28 mmol) in DCM (5 ml) was treated with tert-butyl 2-aminopropanoate hydrochloride (227.1 mg; 1.24 mmol) and polymer supported carbonate (150 mg) followed by polymer supported triacetoxy borohydride (150 mg). After stirring for 18 hours the mixture was filtered and the solvent removed in vacuo. The residue was purified by column chromatography (silica) eluting with petroleum ether containing increasing amounts of EtOAc to give tert-butyl 2-(4-(6-((cyclopropylmethyl)(propyl)amino)pyrimidine-4-carboxamido)-3-methylbenzylamino)propanoate which was used directly without any further purification. The residue was taken up into DCM (4.5 ml) and TFA (0.5 ml) added. After stirring at RT for 2 hours the solvent was removed in vacuo. The residue was taken up into dilute HCl and precipitated by basification to pH 3-4. The solid was removed by filtration, washed with water and dried to give the title compound as a white solid (85 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399448B2
Source datasetuspto-grants-2013_03
ORD IDord-0e0c0c2ccd4c466b9fe22a86999c6892
Source noteuspto-grants-2013_03