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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2358865생성일: 2026년 10월 26일

2-Amino-2-methyl-1-propanol → 3-Anilino-n-(2-hydroxy-1,1-dimethylethyl)-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridine-2-carboxamide

https://huagongshe.com/reaction/2358865

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-2-methyl-1-propanolHCID 11807—
반응물Ethyl 3-(phenylamino)-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridine-2-carboxylateHCID 9865198—
생성물3-Anilino-n-(2-hydroxy-1,1-dimethylethyl)-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridine-2-carboxamideHCID 6845670516%

반응 단계

A mixture of Example 1 and 2-amino-2-methyl-1-propanol (1.22 mL, 13 mmol) was heated at 150° C. for 16 h. The mixture was partitioned between DCM (60 mL) and 10% citric acid (75 mL). The aqueous phase was extracted with DCM (20 mL). The combined organics were dried (Na2SO4) and concentrated in vacuo. Purification by column chromatography (silica, 40% EtOAc in DCM) gave the title compound as a pale brown solid (45 mg, 16%). δH (CDCl3) 8.44 (1H, br s), 7.56-7.46 (3H, m), 7.34-7.31 (2H, m), 7.26-7.20 (3H, m), 7.03-6.96 (3H, m), 6.33 (1H, d, J 9.7 Hz), 5.65 (1H, br s), 4.21-4.18 (1H, br m), 3.49 (2H, d, J 5.5 Hz), 1.18 (6H, s). LCMS (ES+) 434 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07763729B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-3a54ddb796144725a35cf7772c5af1a1
출처 메모uspto-grants-2010_07