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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2204834생성일: 2026년 10월 26일

2-Furancarboxylic acid, hydrazide → 4-[5-amino-6-[5-(2-furyl)-1,3,4-oxadiazol-2-yl]pyrazin-2-yl]-N,N-dimethyl-benzamide

https://huagongshe.com/reaction/2204834

반응식

참여 물질

역할이름HCID투입량
반응물2-Furancarboxylic acid, hydrazideHCID 18731—
반응물Triphenylphosphine dibromideHCID 70579—
반응물DiisopropylethylamineHCID 81531—
반응물3-Amino-6-[4-(dimethylcarbamoyl)phenyl]pyrazine-2-carboxylic acidHCID 59471750—
용매AcetonitrileHCID 6342—
생성물4-[5-amino-6-[5-(2-furyl)-1,3,4-oxadiazol-2-yl]pyrazin-2-yl]-N,N-dimethyl-benzamideHCID 5947170551.3%

반응 단계

Dibromo(triphenyl)phosphorane was added to a solution of 3-amino-6-[4-(dimethylcarbamoyl)phenyl]pyrazine-2-carboxylic acid (100 mg, 0.35 mmol) and furan 2-carbohydrazide (44.1 mg, 0.35 mmol) in acetonitrile (3.0 mL) at room temperature. Bright yellow solution observed. The resulting solution was stirred at room temperature for 30 min. After this time, DIPEA (304 μL, 1.75 mmol) was added dropwise and the reaction mixture stirred at room temperature for 30 min. The reaction mixture was filtered to leave a yellow solid. The solid was purified by reverse phase preparative HPLC [Waters Sunfire C18, 10 mM, 100 Å column, gradient 10%-95% B (solvent A: 0.05% TFA in water; solvent B: CH3CN) over 16 minutes at 25 mL/min]. Product fractions were freeze dried to give the product as a yellow solid (67.6 mg, 51% yield); 1H NMR (400.0 MHz, DMSO) d 2.97 (m, 6H), 6.87 (m, 1H), 7.54-7.56 (m, 3H), 7.57 (br s, 2H), 8.15 (m, 3H) and 8.98 (1H, s) ppm; MS (ES+) 377.17

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09365557B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-4aadd96f21c7426891ae623387bbe91c
출처 메모uspto-grants-2016_06