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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371468Generated: October 26, 2026

Triethylamine → N-[4-[4-(2,4-Diamino-6-propyl-5-pyrimidinyl)-1-piperazinyl]benzoyl]-L-glutamic acid, diethyl ester

https://huagongshe.com/reaction/371468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantGlutamic acid diethyl ester hydrochlorideHCID 73960—
ReactantDiethyl cyanophosphonateHCID 76257—
Reactant4-[4-(2,4-Diamino-6-propyl-5-pyrimidinyl]-1-piperazinyl]benzoic acidHCID 13478350—
SolventDimethylformamideHCID 6228—
ProductN-[4-[4-(2,4-Diamino-6-propyl-5-pyrimidinyl)-1-piperazinyl]benzoyl]-L-glutamic acid, diethyl esterHCID 1347834438.5%

Reaction Steps

A mixture of 3.2 g (0.0091 mole) of 4-[4-(2,4-diamino-6-propyl-5-pyrimidinyl]-1-piperazinyl]benzoic acid, 4.9 g (0.030 mole) of diethyl phosphorocyanidate and 4.2 ml (0.030 mole) of triethylamine in 200 ml of of N,N-dimethylformamide (dried over 4 Å molecular sieves overnight) was stirred at room temperature for two hours. To the resulting clear solution was added a mixture of 2.4 g (0.010 mole) of diethyl glutamate hydrochloride and 1.4 ml (0.010 mole) of triethylamine in 10 ml of N,N-dimethylformamide, and the solution was stirred for another hour. The solvent was removed under high vacuum (0.1 mm, dry ice-2-propanol trap) at 40° C. The gummy residue was poured into 100 ml of ice water. The solid was collected and recrystallized from N,N-dimethylformamide to give 1.9 g of the product as an off-white powder; mp 175°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04532240
Source datasetuspto-grants-1985_07
ORD IDord-cfeba9dfe18b4c19a834bff7925160de
Source noteuspto-grants-1985_07