Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl formate → Methyl 3-(4-oxo-2-thioxo-1,2,3,4-tetrahydro-5-pyrimidinyl)propanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl formate | HCID 7865 | — |
| 반응물 | Dimethyl Glutarate | HCID 14242 | — |
| 반응물 | Thiourea | HCID 2723790 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | tert-Butyl methyl ether | HCID 15413 | — |
| 생성물 | Methyl 3-(4-oxo-2-thioxo-1,2,3,4-tetrahydro-5-pyrimidinyl)propanoate | HCID 86666200 | 30.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09174968B2 |
| 출처 데이터셋 | uspto-grants-2015_11 |
| ORD ID | ord-31d966fc43d943ff85f9fced238701b1 |
| 출처 메모 | uspto-grants-2015_11 |