Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58282생성일: 2026년 10월 24일
Ethyl Acetate → 7-(1-aminoethyl)-6-(3-fluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one
https://huagongshe.com/ko/reaction/58282
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Trimethylphosphine | HCID 68983 | — |
| 반응물 | 7-(1-azidoethyl)-6-(3-fluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one | HCID 58111402 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 7-(1-aminoethyl)-6-(3-fluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one | HCID 58111399 | 98.1% |
반응 단계
To a stirred solution of 7-(1-azidoethyl)-6-(3-fluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one (0.14 g, 0.42 mmol) (1st peak from chiral separation) in tetrahydrofuran (3 mL) and water (0.5 mL) was added 1.00 M of trimethylphosphine in tetrahydrofuran (0.52 mL, 0.52 mmol), and the mixture was stirred at room temperature for 1 hour. To the mixtures were added ethyl acetate and the mixtures were extracted with aqueous 1 N HCl solution (three times). The combined extracts were neutralized with solid NaHCO3, and extracted with dichloromethane (three times). The combined organic layers were washed with brine, dried over MgSO4, and concentrated to give the crude product (0.125 g) used directly in next step. LCMS calculated for C15H15FN3OS (M+H)+: m/z=304.1. Found: 304.0.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434746B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-c887e060cf974d9988a774b6927d528b |
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| 출처 메모 | uspto-grants-2016_09 |
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