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HRID 371468作成日:2026年10月26日

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

https://huagongshe.com/reaction/371468

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Glutamic acid diethyl ester hydrochlorideHCID 73960—
反応物Diethyl cyanophosphonateHCID 76257—
反応物4-[4-(2,4-Diamino-6-propyl-5-pyrimidinyl]-1-piperazinyl]benzoic acidHCID 13478350—
溶媒DimethylformamideHCID 6228—
生成物N-[4-[4-(2,4-Diamino-6-propyl-5-pyrimidinyl)-1-piperazinyl]benzoyl]-L-glutamic acid, diethyl esterHCID 1347834438.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04532240
出典データセットuspto-grants-1985_07
ORD IDord-cfeba9dfe18b4c19a834bff7925160de
出典メモuspto-grants-1985_07