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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73205생성일: 2026년 10월 23일

Phenylsilane → 5-Phenyl-3-(tetrahydro-thiopyran-4-ylamino)-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/73205

반응식

참여 물질

역할이름HCID투입량
반응물PhenylsilaneHCID 12752—
반응물Tetrahydrothiopyran-4-oneHCID 66173—
반응물Methyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
촉매Dibutyltin dichlorideHCID 12688—
용매TetrahydrofuranHCID 8028—
생성물5-Phenyl-3-(tetrahydro-thiopyran-4-ylamino)-thiophene-2-carboxylic acid methyl esterHCID 5975237456.5%

반응 단계

Reductive amination of 3-amino-5-phenyl-thiophene-2-carboxylic acid methyl ester (0.933 g, 4.0 mmol) and tetrahydro-thiopyran-4-one (0.464 g, 4.0 mmol) in THF (1.0 mL) employing Bu2SnCl2 (60.5 mg, 0.2 mmol) and PhSiH3 (0.476 g, 0.542 mL) was carried out as described for example 13, step 1 gave 5-phenyl-3-(tetrahydro-thiopyran-4-ylamino)-thiophene-2-carboxylic acid methyl ester (0.753 g, 56.3%). NMR 1H (CDCl3, 400 MHz): 7.64-7.6 (m, 2H), 7.44-7.34 (m, 3H), 6.9 (brm, 1H), 6.81 (brs, 1H), 3.84 (s, 3H), 3.5-3.4 (m, 1H), 2.85-2.7 (m, 4H), 2.4-2.25 (m, 2H), 1.85-1.7 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829030B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9887b9a5d4de4344accb803ab0a9f125
출처 메모uspto-grants-2014_09