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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 629721생성일: 2026년 10월 24일

Phenylacetylene → tert-butyl (2R,5R)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]-5-[(4-phenyl-1H-1,2,3-triazol-1-yl)methyl]morpholine-4-carboxylate

https://huagongshe.com/ko/reaction/629721

반응식

참여 물질

역할이름HCID투입량
반응물PhenylacetyleneHCID 10821—
반응물DiisopropylethylamineHCID 81531—
반응물tert-butyl (2R,5R)-5-(azidomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylateHCID 86726323—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl (2R,5R)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]-5-[(4-phenyl-1H-1,2,3-triazol-1-yl)methyl]morpholine-4-carboxylateHCID 86726324—

반응 조건

온도70 °C

반응 단계

To a solution of tert-butyl (2R,5R)-5-(azidomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-β-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylate (1 eq.) in tetrahydrofuran (0.033M) were added phenylacetylene (3.9 eq.) and Hunig's base (5 eq.). Nitrogen was then bubbled for 5 minutes through the reaction mixture which was placed in a sealed tube. Copper(I) iodide (1.5 eq.) was added to the reaction mixture and the temperature was raised to 70° C. for 16 hrs. The reaction mixture was evaporated to dryness and the evaporation residue was purified by automated silica gel flash chromatography system eluted with a gradient 0% to 10% of MeOH/CH2Cl2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315475B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-cc0a8d29250a403d9020ce494a36b21e
출처 메모uspto-grants-2016_04