Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3439생성일: 2026년 10월 23일
Phenyl isocyanate → 3-[6-(2,6-Dichlorophenyl)-2-{[4-(diethylamino)butyl]amino}pyrido[2,3-d]pyrimidin-7-yl]-1-phenylurea
https://huagongshe.com/ko/reaction/3439
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenyl isocyanate | HCID 7672 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 6-(2,6-dichlorophenyl)-2-N-[4-(diethylamino)butyl]pyrido[2,3-d]pyrimidine-2,7-diamine | HCID 5328133 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-[6-(2,6-Dichlorophenyl)-2-{[4-(diethylamino)butyl]amino}pyrido[2,3-d]pyrimidin-7-yl]-1-phenylurea | HCID 5328137 | 66.4% |
반응 단계
To a solution of 6-(2,6-dichlorophenyl)-N2 -(4-diethylamino-butyl)-pyrido[2,3-d]pyrimidine-2,7-diamine (1.0 g) from Example 53 in DMF (15 mL) was added one equivalent of 60% sodium hydride suspension (0.93 g). After stirring for approximately 1 hour at room temperature, one equivalent of phenyl isocyanate (0.275 g) was added, and the reaction was monitored by thin layer chromatography. After approximately 24 hours, the solvent was removed in vacuo. The residue was dissolved in ethyl acetate, and this solution was washed several times, first with water and then a saturated solution of sodium chloride. The ethyl acetate layer was dried with magnesium sulfate and concentrated in vacuo. Chromatography of the residue over silica gel using ethyl acetate:methanol: triethylamine (90:10:1) followed by ethyl acetate: ethanol:triethylamine (9:2:1) gave 0.8461 g of the title compound 1-[6-(2,6-dichlorophenyl)-2-(4-diethylamino-butylamino)-pyrido[2,3-d]pyrimidin-7-yl]-3-phenyl-urea, ESMS (20/80 MeOH/CH3CN+0.1% AcOH): M+ +H=552 (Base), 433; mp 81°-87.5° 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-e67c6fe74c75494e9570b2bde6a06c78 |
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| 출처 메모 | uspto-grants-1998_03 |
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