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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 847271생성일: 2026년 10월 24일

4-Methylmorpholine → Tyrosine N'-Boc-hydrazide

https://huagongshe.com/ko/reaction/847271

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물tert-Butyl carbazateHCID 70091—
반응물N-benzyloxycarbonyl-l-tyrosineHCID 712438—
용매TetrahydrofuranHCID 8028—
생성물Tyrosine N'-Boc-hydrazideHCID 22845507—

반응 단계

A solution of CBZ-L-tyrosine (3.00 gm, 9.11 mmoles), N-methylmorpholine (0.92 gm, 1.00 ml, 9.11 mmoles) in 100 ml dry tetrahydrofuran (THF) was cooled to 0° C. under nitrogen. 2,2,2-Trichloro-1,1-dimethylethylchloroformate (2.18 gm, 9.11 mmoles) was added to the cold solution. After 5 minutes stirring, a solution of t-butyl carbazate (1.20 gm, 9.11 mmoles) in 20 ml dry THF was cooled to 0° C. and added to the reaction mixture. The mixture was allowed to warm slowly to room temperature and was stirred for about 18 hours. The solvent was removed by rotary evaporation and the residue was partitioned between chloroform and water and the layers separated. The organic layer was washed with saturated NaCl dried over Na2SO4, filtered, and solvent evaporated to yield the crude protected product. The CBZ-protected product, CBZ-tyrosine N'-Boc-hydrazide, was purified on silica gel via flash chromatography using a mixture of petroleum ether and ethyl acetate (1:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05140104
출처 데이터셋uspto-grants-1992_08
ORD IDord-d87efd99412042b991f4e3eb41a8f29a
출처 메모uspto-grants-1992_08