Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 605695생성일: 2026년 10월 27일
Butyl bromide → N-butyl-1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-amine
https://huagongshe.com/reaction/605695
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butyl bromide | HCID 8002 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-({3,4-Difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-amine | HCID 16221889 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-butyl-1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-amine | HCID 16222095 | 37.1% |
반응 단계
To a solution of 1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-amine (0.09 M in acetonitrile, 500 μL, 0.045 mmol), prepared using procedures similar to those described in Example 2, was added triethylamine (20 μL, 0.135 mmol) and n-butylbromide (6.14 μL, 0.054 mmol) followed by additional acetonitrile (1.0 mL). The reaction mixture was stirred at room temperature for 16 h, at which time it was purified directly by reverse phase HPLC to afford the title compound (8.4 mg). 1H NMR (400 MHz, CDCl3): 8.50 (s, 1H), 7.39 (dd, 1H), 7.32 (dd, 1H), 7.13-7.09 (m, 1H), 6.84-6.77 (m, 1H), 6.63-6.57 (m, 1H), 4.35 (br s, 2H), 4.00 (br s, 1H), 3.87 (br s, 1H), 3.74-3.68 (m, 1H), 3.20 (br s, 3.5H), 2.56 (t, 2H), 2.03 (s, 2H), 1.50-1.42 (m, 2H), 1.39-1.29 (m, 2H), 0.91 (t, 3H). MS (EI) for C20H21F3IN3O: 504 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07915250B2 |
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| 출처 데이터셋 | uspto-grants-2011_03 |
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| ORD ID | ord-c24c8d447a37446fa4622011c5ab4cc8 |
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| 출처 메모 | uspto-grants-2011_03 |
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