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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1807997생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1807997

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 번호US08357718B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-8c539e10f72a412ebbcd3e3476afcca5
출처 메모uspto-grants-2013_01