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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572292생성일: 2026년 10월 24일

3-Amino-4-chloropyridine → HCID 25211384, 화합물

https://huagongshe.com/ko/reaction/572292

반응식

참여 물질

역할이름HCID투입량
반응물3-Amino-4-chloropyridineHCID 581932—
반응물HCID 86628351HCID 86628351—
용매TetrahydrofuranHCID 8028—
생성물HCID 25211384HCID 2521138416%

반응 단계

A solution of 3-amino-4-chloropyridine (129 mg, 1.0 mmol) in THF (2 mL) was treated with solid 5-(4-methyl-5-trifluoromethyl-isoxazol-3-yl)-thiophene-2-carbonyl chloride (148 mg, 0.5 mmol, as prepared in Example 2 Method B) and allowed to stir for 1 hr. The reaction was then evaporated and the residue chromatographed on silica gel with EtOAc/hexanes (70%) as eluant to afford product as a colorless solid (31 mg, 16%). 1H NMR (CDCl3) 2.39 (d, J=1.5, 3H), 7.39 (d, J=5.3, 1H), 7.56 (d, J=7.56, 4.1, 1H), 7.72 (d, J=4.1, 1H), 8.22 (s, 1H), 8.33 (d, J=4.7, 1H), 9.61 (s, 1H). 13C NMR 8.0, 114.8, 118.7 (q, J=271), 129.0, 129, 7, 132.9, 134.6, 140.5, 143.8, 146.1, 157.7, 159.0, 19F NMR −63.1. LC/MS 6.34 min, [M+1]+ 388.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029397B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-65632bb6ba0c4b71b49af4f9368c64c8
출처 메모uspto-grants-2015_05