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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1483214생성일: 2026년 10월 26일

Sodium Cyanate → 6-Ethyl-2-ureido-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamide

https://huagongshe.com/reaction/1483214

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CyanateHCID 517096—
반응물2-Amino-6-ethyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamideHCID 614439—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물6-Ethyl-2-ureido-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamideHCID 11827012423.3%

반응 단계

To a stirred mixture of compound F4 (451 mg, 2.00 mmol) in acetic acid (6 mL) at room temperature was added a solution of sodium cyanate (169 mg, 2.60 mmol) in water (2.5 mL) dropwise over 2 min. After addition, the reaction mixture was stirred for another 2 h and then concentrated under reduced pressure. The resulting residue was mixed with saturated aqueous sodium bicarbonate (50 mL) and extracted with methylene chloride (3×150 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The resulting residue was purified by flash column chromatography on silica gel eluting with methanol/methylene chloride (15:85) to afford compound M1 as a yellow solid (125 mg, 23%): 1H NMR (300 MHz, DMSO-d6) δ 10.45 (s, 1H), 7.31 (bs, 1H), 6.77 (bs, 3H), 3.41 (s, 2H), 2.73 (d, J=4.8 Hz, 2H), 2.63 (d, J=4.8 Hz, 2H), 2.50-2.45 (m, 2H), 1.06 (t, J=7.0 Hz, 3H). MS (M+H) 269.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09416141B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-708cb3855ac8442382312e0e3e061088
출처 메모uspto-grants-2016_08