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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenylacetylene | HCID 10821 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | tert-butyl (2R,5R)-5-(azidomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylate | HCID 86726323 | — |
| 촉매 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 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 | HCID 86726324 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09315475B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-cc0a8d29250a403d9020ce494a36b21e |
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| 출처 메모 | uspto-grants-2016_04 |
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