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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1906710생성일: 2026년 10월 25일

Triethylamine → 4-Methyl-1,3-dioxol-2-one-5-ylmethyl(S)N-(t-Butoxycarbonyl)-3-hydroxy-alpha-methyltyrosinate

https://huagongshe.com/reaction/1906710

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(Bromomethyl)-5-methyl-1,3-dioxol-2-oneHCID 10774141—
반응물(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acidHCID 15719345—
용매DimethylformamideHCID 6228—
생성물4-Methyl-1,3-dioxol-2-one-5-ylmethyl(S)N-(t-Butoxycarbonyl)-3-hydroxy-alpha-methyltyrosinateHCID 13171508731%

반응 단계

A solution of N-(t-butoxycarbonyl)-3-hydroxy-α-methyltyrosine (760 mg, 2.44 mmol), triethylamine (263 mg, 2.60 mmol) and 4-bromomethyl-5-methyl-1,3-dioxol-2-one (500 mg, 2.60 mmol) in dimethylformamide, 10 mL, is stirred at 60° C. for 3 hours under nitrogen. Most of the dimethylformamide is removed at 50°-60° C. and 0.1 mm and the residue is partitioned between saturated sodium bicarbonate solution, 10 mL, and ethyl acetate, 50 mL. The ethyl acetate extract is washed with water saturated with sodium sulfate, filtered and concentrated at 40°-45° C. and 15 mm. Flash chromatography of the residue over 40 g of silica gel 60 (230-400 mesh) with 3% methanol-97% chloroform as eluent affords 320 mg of the desired ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04654331
출처 데이터셋uspto-grants-1987_03
ORD IDord-36018ca2a034414b8916320a13fbcf43
출처 메모uspto-grants-1987_03