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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1763731생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → Carbobenzyloxytryptophylserine methyl ester

https://huagongshe.com/reaction/1763731

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물benzyloxycarbonyl-L-tryptophanHCID 101176—
반응물L-Serine, methyl ester, hydrochloride (1:1)HCID 2723730—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물Carbobenzyloxytryptophylserine methyl esterHCID 12821032—

반응 단계

L-Serine methyl ester hydrochloride, 5 g., is dissolved in 75 ml. of dimethylformamide and the solution cooled in an ice bath. Triethylamine, 4.9 ml., is added then 11.9 g. of Nα -benzyloxycarbonyl-L-tryptophan, 5.25 g. of 1-hydroxybenztriazole and finally 8.0 g. of dicyclohexylcarbodiimide. The reaction is stirred with ice bath cooling overnight, allowing the temperature to rise to room temperature, then an additional twenty-four hours at room temperature. The mixture is filtered and the solid washed with dimethylformamide. The filtrate is evaporated under reduced pressure and the residue dissolved in ethyl acetate and washed with dilute hydrochloric acid, saturated salt solution, three times with 5% sodium bicarbonate solution, saturated salt solution, and finally with water. The ethyl acetate solution is then dried over magnesium sulfate and evaporated. The residue is crystallized from 250 ml. of benzene and then from ethyl acetate and petroleum ether; 12.5 g.; m.p. 133°-135° C.; [α]D23 -12.4° (c 2, methanol); ultraviolet in methanol λmax 290 E11 115; λmax 281 E11 131; λmax 274 E11 122.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04111923
출처 데이터셋uspto-grants-1978_09
ORD IDord-99785dc6ae3c4c05a4d7a562038650bd
출처 메모uspto-grants-1978_09