Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanethiol → 2-Amino-4-fluoromethyl-6-methylthiopyrimidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanethiol | HCID 878 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | 4-Fluoro-6-(fluoromethyl)pyrimidin-2-amine | HCID 20153498 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2-Amino-4-fluoromethyl-6-methylthiopyrimidine | HCID 20153491 | — |
반응 단계
A mixture of 1.0 part of 2-amino-4-fluoro-6-fluoromethylpyrimidine, 3.0 parts of methanethiol and 50 parts of dry tetrahydrofuran was stirred at 5° C. whilst a solution of 0.16 parts of sodium in 20 parts of dry methanol was added dropwise. The temperature was kept below 10° C. with ice-bath cooling. When the addition was complete, stirring was continued for 1 hour. The resulting solution was evaporated and the residue was diluted with water and extracted three times with 50 parts of ether. The ethereal solutions were combined and dried (MgSO4). The solvent was evaporated and the crude product was purified by recrystallisation from carbon tetrachloride to give 2-amino-4-fluoromethyl-6-methylthiopyrimidine m.p. 95°-97° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04723006 |
| 출처 데이터셋 | uspto-grants-1988_02 |
| ORD ID | ord-2890b78e01af42029f6cf55bc787a012 |
| 출처 메모 | uspto-grants-1988_02 |