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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978417Generated: October 31, 2026

Diethyl cyanophosphonate → HCID 70248359, compound

https://huagongshe.com/reaction/1978417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl cyanophosphonateHCID 76257—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
ReactantHCID 53673182HCID 53673182—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 70248359HCID 70248359—

Reaction Steps

While 0.708 g (2.898 mM) of 3-(5-thia-1,8b-diazaacenaphthylen-4-yl)acrylic acid, 0.68 g (3.19 mM) of 1-(tert-butoxycarbonyl)piperidin-4-ylmethylamine, and 0.48 ml (3.48 mM) of triethylamine were stirred together in 10 ml of N,N-dimethylformamide, 0.53 ml (3.48 mM) of diethyl cyanophosphate was added dropwise at room temperature and the mixture was stirred at the prevailing temperature overnight. This reaction mixture was poured in aqueous solution of sodium hydrogen carbonate and extracted with 3 portions of ethyl acetate. The organic layers were pooled and dried over MgSO4 and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate to ethyl acetate-methanol=9/1) to provide crude N-[1-(tert-butoxycarbonyl)piperidin-4-ylmethyl]-3-(5-thia-1,8b-diazaacenaphthylen-4-yl)acrylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235731B1
Source datasetuspto-grants-2001_05
ORD IDord-2451e341d81d486ab078c134dc563ae7
Source noteuspto-grants-2001_05