Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243813생성일: 2026년 10월 24일
Diisopropylethylamine → 1-(5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenyl)-3-((1S,2R)-1-hydroxy-2,3-dihydro-1H-indene-2-yl)urea
https://huagongshe.com/ko/reaction/243813
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | L-Tartaric acid | HCID 444305 | — |
| 반응물 | rac-(1R,2S)-2-amino-2,3-dihydro-1H-inden-1-ol | HCID 11008081 | — |
| 반응물 | 2,2,2-Trichloroethyl 5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenylcarbamate | HCID 68107458 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 1-(5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenyl)-3-((1S,2R)-1-hydroxy-2,3-dihydro-1H-indene-2-yl)urea | HCID 68107804 | 51% |
반응 단계
To a solution of 2,2,2-trichloroethyl 5-tert-butyl-3-(2-cyanopropan-2-yl)-2-methoxyphenylcarbamate (0.086 g, 0.203 mmol) and (1S,2R)-2-amino-2,3-dihydro-1H-indene-1-ol.L-tartaric acid salt (0.067 g, 0.223 mmol) in acetonitrile (0.8 mL), N,N-diisopropylethylamine (0.058 mL, 0.333 mmol) was added, the mixture was stirred overnight at 110° C. The reaction mixture was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=10/90-60/40) to obtain 0.044 g of the captioned compound (51% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08653304B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-bcc932fdcde14f20ba571ba2466d1d37 |
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| 출처 메모 | uspto-grants-2014_02 |
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