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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 705852생성일: 2026년 10월 25일

Methyl formate → Methyl 3-(4-oxo-2-thioxo-1,2,3,4-tetrahydro-5-pyrimidinyl)propanoate

https://huagongshe.com/reaction/705852

반응식

참여 물질

역할이름HCID투입량
반응물Methyl formateHCID 7865—
반응물Dimethyl GlutarateHCID 14242—
반응물ThioureaHCID 2723790—
반응물Potassium tert-butoxideHCID 23665647—
용매MethanolHCID 887—
용매tert-Butyl methyl etherHCID 15413—
생성물Methyl 3-(4-oxo-2-thioxo-1,2,3,4-tetrahydro-5-pyrimidinyl)propanoateHCID 8666620030.2%

반응 단계

To a suspension of potassium tert-butoxide (7.29 g, 64.9 mmol) in t-butylmethyl ether (100 mL) was added a solution of dimethyl pentanedioate (5.2 g, 32.5 mmol) and methyl formate (1.950 g, 32.5 mmol) in t-butylmethyl ether (50 mL). The mixture was stirred overnight and concentrated to dryness afford the yellow oil. The oil was dissolved in methanol (80 mL), to which thiourea (2.72 g, 35.7 mmol) was added. The mixture was heated to reflux overnight. The result mixture was concentrated and dissolved in water, adjust pH to 3 with AcOH. The solution was extracted with DCM three times. The combined organic layers were dried over Na2SO4, filtered and concentrated to afford the title compound (2.1 g, 9.80 mmol, 30.2% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09174968B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-31d966fc43d943ff85f9fced238701b1
출처 메모uspto-grants-2015_11