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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 446740생성일: 2026년 10월 25일

Triphenylphosphine → 3-(1-(4-((R)-tetrahydrofuran-3-yloxy)-2,3-difluorophenyl)-1H-tetrazol-5-yl)-5-bromopyridin-2-amine

https://huagongshe.com/reaction/446740

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물(S)-(+)-3-HydroxytetrahydrofuranHCID 2733227—
반응물4-(5-(2-amino-5-bromopyridin-3-yl)-1H-tetrazol-1-yl)-2,3-difluorophenolHCID 58293790—
용매TetrahydrofuranHCID 8028—
생성물3-(1-(4-((R)-tetrahydrofuran-3-yloxy)-2,3-difluorophenyl)-1H-tetrazol-5-yl)-5-bromopyridin-2-amineHCID 5829377192.5%

반응 단계

A solution of Compound 1086 (90 mg, 0.2438 mmol), triphenylphosphine (76.74 mg, 0.2926 mmol), diisoproplylazodicarboxylate (59.17 mg, 56.68 μL, 0.2926 mmol), and (S)-tetrahydrofuran-3-ol (25.78 mg, 0.2926 mmol) in THF (90 μL) was heated at 70° C. for 10 minutes under microwave irradiation. The reaction was quenched with ammonium chloride (satd') and extracted with EtOAc. The organics were washed with 1 M NaOH (2×), brine, dried over sodium sulfate, and concentrated under vacuum. The residue was chromatographed over silica gel (0-50% EtOAc/hexanes gradient) to give 3-(1-(4-((R)-tetrahydrofuran-3-yloxy)-2,3-difluorophenyl)-1H-tetrazol-5-yl)-5-bromopyridin-2-amine (Compound 1090, 99 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481524B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-5ea3c27186d64bf1b1e51b79fc6b0e78
출처 메모uspto-grants-2013_07