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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371456생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/371456

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Glutamic acid diethyl ester hydrochlorideHCID 73960—
반응물Diethyl cyanophosphonateHCID 76257—
반응물4-[4-(2,4-Diamino-6-methyl-5-pyrimidinyl)-1-piperazinyl]benzoic acid hydrochlorideHCID 70412613—
용매DimethylformamideHCID 6228—
생성물N-[4-[4-(2,4-Diamino-6-methyl-5-pyrimidinyl)-1-piperazinyl]benzoyl]-L-glutamic acid diethyl esterHCID 1347833766.8%

반응 단계

A mixture of 4.27 g (0.01137 mole) of 4-[4-(2,4-diamino-6-methyl-5-pyrimidinyl)-1-piperazinyl]benzoic acid hydrochloride, 6.12 g (0.0375 mole) of diethyl phosphorocyanidate and 7.0 ml (0.050 mole) of triethylamine in 300 ml of previously dried dimethylformamide was stirred at room temperature for five hours and then at 80° C. for five minutes. The solution was cooled to room temperature, and a solution of 3.00 g (0.0125 mole) of L-glutamic acid diethyl ester hydrochloride and 1.74 ml (0.0125 mole) of triethylamine was added. The resulting mixture was stirred for two hours at room temperature. The solvent was removed under high vacuum at 40° C. and the gummy residue partitioned between 500 ml of dichloromethane and 500 ml of 5% sodium bicarbonate solution. The organic layer was separated, washed with water and then with saturated sodium chloride solution and dried over magnesium sulfate. The dried solution was concentrated in vacuo to give a yellow solid. Recrystallization from acetonitrile gave 3.9 g of the product as a tan solid, mp 224° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04532240
출처 데이터셋uspto-grants-1985_07
ORD IDord-6a744a14880343868338d153caee0a75
출처 메모uspto-grants-1985_07