돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 371468생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/371468

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Glutamic acid diethyl ester hydrochlorideHCID 73960—
반응물Diethyl cyanophosphonateHCID 76257—
반응물4-[4-(2,4-Diamino-6-propyl-5-pyrimidinyl]-1-piperazinyl]benzoic acidHCID 13478350—
용매DimethylformamideHCID 6228—
생성물N-[4-[4-(2,4-Diamino-6-propyl-5-pyrimidinyl)-1-piperazinyl]benzoyl]-L-glutamic acid, diethyl esterHCID 1347834438.5%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04532240
출처 데이터셋uspto-grants-1985_07
ORD IDord-cfeba9dfe18b4c19a834bff7925160de
출처 메모uspto-grants-1985_07