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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53163Generated: October 30, 2026

Benzoyl chloride → 2-[4-(N,N-Dimethylamino)-piperidino]-8-[N-benzyl-N-(3-benzoylaminopropyl)-amino]-4-morpholino-pyrimido[5,4-d]-pyrimidine

https://huagongshe.com/reaction/53163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant2-[4-(N,N-dimethylamino)-piperidino]-8-[N-benzyl-N-(3-aminopropyl)-amino]-4-morpholino-pyrimido[5,4-d]pyrimidineHCID 19961998—
SolventDichloromethaneHCID 6344—
Product2-[4-(N,N-Dimethylamino)-piperidino]-8-[N-benzyl-N-(3-benzoylaminopropyl)-amino]-4-morpholino-pyrimido[5,4-d]-pyrimidineHCID 19961981—

Reaction Steps

0.75 g of 2-[4-(N,N-dimethylamino)-piperidino]-8-[N-benzyl-N-(3-aminopropyl)-amino]-4-morpholino-pyrimido[5,4-d]pyrimidine are dissolved in 8 ml of methylene chloride and mixed with 0.24 g of benzoyl chloride and 0.3 g of triethylamine in 2 ml of methylene chloride. The reaction mixture is stirred for 12 hours at ambient temperature and then extracted three times with water. The organic phase is dried over sodium sulphate and concentrated by rotary evaporation. The residue is chromatographed over a silica gel column using methylene chloride/methanol=7:3. Yield: 0.7 g (77% of theory) Oil C34H43N9O2 (609.78)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618814
Source datasetuspto-grants-1997_04
ORD IDord-72399ba07a3749c28b19c65fbe9957d7
Source noteuspto-grants-1997_04