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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73195생성일: 2026년 10월 25일

Acetic Acid → 3-(1-Methyl-piperidin-4-ylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/73195

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium HydroxideHCID 14798—
반응물Methyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-Methyl-4-trimethylsilanyloxy-1,2,3,6-tetrahydro-pyridineHCID 10081120—
용매1,1-DichloroethaneHCID 6365—
생성물3-(1-Methyl-piperidin-4-ylamino)-5-phenyl-thiophene-2-carboxylic acid methyl esterHCID 2077574973%

반응 단계

To a stirred solution of methyl-3-amino-5-phenylthiophene-carboxylate (233 mg, 1.0 mmol) and 1-methyl-4-trimethylsilanyloxy-1,2,3,6-tetrahydro-pyridine (370 mg, 2.0 mmol) in dichloroethane (3.0 mL) was added AcOH (0.114 mL, 2.0 eq) and followed addition of NaBH(OAc)3 (424 mg, 2.0 mmol) in one portion. The resultant reaction mixture was stirred at RT for weekend, aq. 10% NaOH (until basic) was added, after 30 min, reaction mixture was extracted with dichloromethane. The organic extract was washed with brine and dried. The crude product was purified on silica gel column using 20% EtOAc/hexane for unreacted starting material followed by CHCl3/MeOH/Et3N (180/16/1) furnished the 3-(1-methyl-piperidin-4-ylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester (240 mg, 73%). NMR 1H (CDCl3, 400 MHz): 7.64-7.6 (m, 2H), 7.43-7.34 (m, 3H), 6.83 (brs, 2H), 3.83 (s, 3H), 3.46-3.4 (m, 1H), 2.82-2.74 (m, 1H), 2.3 (s, 3H), 2.26-2.2 (m, 4H), 1.72-1.62 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829030B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-5108744bbdbd495fb6d10a4012885767
출처 메모uspto-grants-2014_09