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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78655생성일: 2026년 10월 24일

Triethylamine → Ethyl 2-(2-(3-amino-6-(4-(isopropylsulfonyl)phenyl)pyrazine-2-carbonyl)hydrazinyl)-2-oxoacetate

https://huagongshe.com/ko/reaction/78655

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethoxalyl chlorideHCID 20884—
반응물3-Amino-6-(4-isopropylsulfonylphenyl)pyrazine-2-carbohydrazideHCID 59471632—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-(2-(3-amino-6-(4-(isopropylsulfonyl)phenyl)pyrazine-2-carbonyl)hydrazinyl)-2-oxoacetateHCID 5947233058.5%

반응 단계

3-amino-6-(4-isopropylsulfonylphenyl)pyrazine-2-carbohydrazide (2 g, 5.963 mmol) and Et3N (1.810 g, 2.493 mL, 17.89 mmol) were dissolved in THF (128.0 mL) and treated dropwise with ethyl 2-chloro-2-oxo-acetate (814.2 mg, 666.3 μL, 5.963 mmol) at 0° C. The reaction mixture was warmed slowly to room temperature and stirred for 1.5 h. The reaction mixture was filtered and grey solid washed with THF. The filtrate was evaporated to dryness azeotroping with acetonitrile. Then residue was then triturated with acetonitrile to give the product as a yellow solid (1.52 g, 58%); 1H NMR (400 MHZ, DMSO) d 1.19 (m, 6H), 1.32 (m, 3H), 3.34 (m, 1H), 4.32 (m, 2H), 7.88 (m, 2H), 8.56 (m, 2H), 9.07 (s, 1H), 10.95 (s, 1H) and 11.05 (s, 1H) ppm; MS (ES+) 436.32

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841308B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4b4f714610f449a0801f1607f809f9fe
출처 메모uspto-grants-2014_09