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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572057생성일: 2026년 10월 26일

1,2-Dichloroethane → Isobutyric acid N'-(5-fluoro-pyridin-2-yl)-hydrazide

https://huagongshe.com/reaction/572057

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물Isobutyric AcidHCID 6590—
반응물Sodium BicarbonateHCID 516892—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물5-Fluoro-2-hydrazinylpyridineHCID 19916786—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물Isobutyric acid N'-(5-fluoro-pyridin-2-yl)-hydrazideHCID 6697782146%

반응 단계

To a solution of 5-fluoro-2-hydrazinyl-pyridine (for reference procedure see WO 2010/022076, which is incorporated herein by reference in its entirety; 2.08 g, 16.4 mmol), isobutyric acid (1.82 mL, 19.6 mmol), and HOBt hydrate (251 mg, 1.64 mmol) in DCM (50 mL), EDC (3.76 g, 19.6 mmol) was added, and the resulting orange solution was stirred at room temperature for 18 h. Sat. aq. NaHCO3 (50 mL) was added, and the mixture was stirred vigorously for 15 min. The organics were washed with sat. aq. NaHCO3 (50 mL), passed through a hydrophobic frit, and concentrated under vacuum to leave a pale brown solid. The solid was suspended in Et2O (50 mL) and filtered, washing with Et2O (25 mL), to leave a white solid (1.48 g, 46%). The ethereal washings were concentrated under vacuum and the residue suspended in Et2O (10 mL), filtered, washed with Et2O (2×2 mL), to leave a white solid (330 mg, 10%). The solids were combined (1.81 g, 56%). 1H NMR (400 MHz, CDCl3): 1.23 (6H, d), 2.50 (1H, sept), 6.65 (1H, dd), 6.80 (1H, d), 7.29 (1H, ddd), 7.77 (1H, br s), 8.01 (1H, d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029373B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-0dded7e486a14c03993d27337a8ccf42
출처 메모uspto-grants-2015_05