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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2204851생성일: 2026년 10월 27일

Triphenylphosphine dibromide → 5-Bromo-3-(5-(3-methylthiophen-2-yl)-1,3,4-oxadiazol-2-yl)pyrazin-2-amine

https://huagongshe.com/reaction/2204851

반응식

참여 물질

역할이름HCID투입량
반응물Triphenylphosphine dibromideHCID 70579—
반응물DiisopropylethylamineHCID 81531—
반응물3-amino-6-bromo-N'-(3-methylthiophene-2-carbonyl)pyrazine-2-carbohydrazideHCID 59472301—
용매AcetonitrileHCID 6342—
생성물5-Bromo-3-(5-(3-methylthiophen-2-yl)-1,3,4-oxadiazol-2-yl)pyrazin-2-amineHCID 5947182959.3%

반응 단계

To a suspension of 3-amino-6-bromo-N′-(3-methylthiophene-2-carbonyl)pyrazine-2-carbohydrazide (7.85 g, 22.04 mmol) in anhydrous acetonitrile (117.8 mL) cooled in an ice bath was added DIPEA (8.546 g, 11.52 mL, 66.12 mmol) followed by dibromo(triphenyl)phosphorane (12.09 g, 28.65 mmol) portionwise. The resulting suspension was stirred at room temperature for 30 min and the precipitate isolated by filtration and washed with acetonitrile to give the product as a yellow solid (4.42 g, 52% yield); 1H NMR (400 MHz, DMSO) d 2.64 (s, 3H), 7.21 (d, 1H), 7.91 (3H, m) and 8.44 (s, 1H) ppm; MS (ES+) 340.04

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09365557B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-697dc441f44d49d68012f698508f728d
출처 메모uspto-grants-2016_06