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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2204838생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2204838

반응식

참여 물질

역할이름HCID투입량
반응물Triphenylphosphine dibromideHCID 70579—
반응물Thiophene-2-carbohydrazideHCID 73098—
반응물DiisopropylethylamineHCID 81531—
반응물3-Amino-6-bromopyrazine-2-carboxylic acidHCID 18521600—
용매AcetonitrileHCID 6342—
생성물5-Bromo-3-(5-(thiophen-2-yl)-1,3,4-oxadiazol-2-yl)pyrazin-2-amineHCID 5947190858.3%

반응 단계

3-amino-6-bromo-pyrazine-2-carboxylic acid (3.2 g, 14.68 mmol) and thiophene-2-carbohydrazide (2.152 g, 14.68 mmol) were suspended in acetonitrile (48.00 mL) at room temperature and dibromo(triphenyl)phosphorane (24.79 g, 58.72 mmol) was added, followed byadditional acetonitrile (16.00 mL). The reaction mixture turned bright yellow in colour and was stirred at room temperature for 1 h. After this time, the reaction mixture cooled in an icebath and DIPEA (7.209 g, 9.716 mL, 55.78 mmol) was added dropwise. The reaction mixture was stirred in the ice bath for 1 h and then additional DIPEA (2.277 g, 3.069 mL, 17.62 mmol) added and the reaction mixture stirred for left for 30 mins and further DIPEA (1.897 g, 2.557 mL, 14.68 mmol) added. The reaction mixture was stirred for 1 h and then filtered. The solid was washed with ether, isolated and then triturated with acetonitrile and washed with ether to give the product as a yellow solid (2.776 g, 57% yield); 1H NMR (400.0 MHz, DMSO) 7.35 (s, 1H), 7.80 (br s, 2H), 7.98 (m, 1H), 8.04 (m, 1H) and 8.45 (s, 1H); MS (ES+) 326.04

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09365557B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-12757414f3104ed6b08e84142dbb24a8
출처 메모uspto-grants-2016_06