Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-methyl-2-pyrrolidone → 2-(2-Morpholinoethyl)thieno[2,3-d]pyrimidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 반응물 | 2-Morpholinoethylamine | HCID 408285 | — |
| 반응물 | 2-(Methylsulfonyl)thieno[2,3-d]pyrimidine | HCID 21988356 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-(2-Morpholinoethyl)thieno[2,3-d]pyrimidine | HCID 68559142 | 87.6% |
반응 단계
A solution of 2-(methylsulfonyl)thieno[2,3-d]pyrimidine (1.0 g, 4.67 mmol), 4-(2-aminoethyl)morpholine (1.8 g, 14.02 mmol), and 1-methyl-2-pyrrolidinone (1.5 mL) was heated to 100° C. overnight. The reaction mixture was cooled to RT and diluted with EtOAc (200 mL)/water (75 mL). The layers were separated, and the organic layer was washed successively with water (4×75 mL) and brine (1×75 mL). The organic layer was then dried over MgSO4, filtered and concentrated to give (1.2 g) of the crude product. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Redi-Sep pre-packed silica gel column (40 g), eluting with a gradient of 5% to 95% MeOH in DCM to provide the title compound (1.02 g) MS (ES+): 265 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07745449B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-d2b26d6d89424ae8a6597c6c0ad4a804 |
| 출처 메모 | uspto-grants-2010_06 |