Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38925생성일: 2026년 10월 25일
1,1,1-Trifluoro-3-iodopropane → N-{[(2S)-5-Fluoro-7-(methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methyl}-N-(3,3,3-trifluoropropyl)amine
https://huagongshe.com/reaction/38925
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,1,1-Trifluoro-3-iodopropane | HCID 156165 | — |
| 반응물 | [(2S)-5-Fluoro-7-(methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methylamine | HCID 67198473 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-{[(2S)-5-Fluoro-7-(methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methyl}-N-(3,3,3-trifluoropropyl)amine | HCID 44470012 | — |
반응 단계
A mixture of 1-[(2S)-5-fluoro-7-(methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-yl]methaneamine (0.3 g, 1.1 mmol), 1,1,1-trifluoro-3-iodopropane (0.16 ml, 1.4 mmol) K2CO3 (0.32 g, 2.3 mmol) and ACN (4 ml) was heated under microwave radiation at 120° C. for 30 min. The mixture was filtrated and evaporated to dryness and the product was purified by flash column chromatography (EtOAc). Yield: 0.12 g, 31%. The amine was converted to the hydrochloric acid salt and crystallized from MeOH/Et2O. M.p. 233° C. MS m/z (rel. intensity, 70 eV) 357 (M+, 1), 274 (3), 127 (5), 126 (bp), 69 (3). [α]=−53° (MeOH).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524766B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-a2a7245bab0f480fbf5c11acfc863f3a |
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| 출처 메모 | uspto-grants-2013_09 |
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