Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3443생성일: 2026년 10월 24일
Sodium hydride → 3-Tert-butyl-1-[6-(2,6-dichlorophenyl)-2-{[3-(morpholin-4-yl)propyl]amino}pyrido[2,3-d]pyrimidin-7-yl]urea
https://huagongshe.com/ko/reaction/3443
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | tert-Butyl isocyanate | HCID 62412 | — |
| 반응물 | 6-Arylpyrido[2,3-d]pyrimidine deriv. 42 | HCID 5328144 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-Tert-butyl-1-[6-(2,6-dichlorophenyl)-2-{[3-(morpholin-4-yl)propyl]amino}pyrido[2,3-d]pyrimidin-7-yl]urea | HCID 5328145 | 79.8% |
반응 단계
To a solution of 6-(2,6-dichlorophenyl)-N2 -(3-morpholin-4-yl-propyl)-pyrido[2,3-d]pyrimidine-2,7-diamine (1.0 g) from Example 58 in DMF (15 mL) was added one equivalent of 60% sodium hydride suspension (0.92 g). After stirring for approximately 1 hour at room temperature, one equivalent of tert-butyl isocyanate (0.230 g) was added, and the reaction was monitored by thin layer chromatography. After approximately 4 hours, the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and water. The aqueous layer was washed several times with ethyl acetate. The ethyl acetate layers were combined, dried with magnesium sulfate, and concentrated in vacuo. Chromatography of the residue on silica gel using ethyl acetate followed by ethyl acetate:ethanol:triethylamine (18:2:1) gave 0.98 g of the title compound 1-tert-butyl-3-[6-(2,6-dichlorophenyl)-2-(3-morpholin-4-yl-propylamino)-pyrido[2,3-d]pyrimidin-7-yl]-urea, CIMS (1% NH3 in CH4): 532=M+ +H, 531=M+,433, 84 (Base); mp 236°-240° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05733913 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-ede167eccc134bd3a388eacac4ece473 |
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| 출처 메모 | uspto-grants-1998_03 |
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