Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273297생성일: 2026년 10월 26일
Imatinib amine → 4-(dichloromethyl)-N-(4-methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)benzamide
https://huagongshe.com/reaction/273297
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Imatinib amine | HCID 9965429 | — |
| 반응물 | Methyl 4-(dichloromethyl)benzoate | HCID 10798892 | — |
| 반응물 | Trimethylaluminum | HCID 16682925 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-(dichloromethyl)-N-(4-methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)benzamide | HCID 67533795 | — |
반응 단계
To a suspension of 4-methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benzene-1,3-diamine (2.00 g mg, 7.21 mmol) in toluene (22 ml) at 45° C. under an atmosphere of argon is added sequentially 4-dichloromethyl-benzoic acid methyl ester (1.90 g, 8.67 mmol) and AlMe3 (2 M in toluene, 12.6 ml, 25.2 mmol). The resulting brown solution is stirred at 45° C. for a period of 3.5 hrs. The reaction mixture is then cooled to 0° C. and quenched by slow addition of a saturated aqueous solution of Rochelle salt (70 ml) which causes the precipitation of the crude product. t-Butyl methyl ether (150 ml) and methylene chloride (100 ml) are added sequentially to the suspension which are then washed with aqueous saturated NaHCO3 (100 ml) and aqueous saturated NaCl (100 ml). The aqueous phases are back-extracted with t-butyl methyl ether (100 ml). The crude product, which is contained in the combined organic phases, is filtered off with suction, washed with t-butyl methyl ether and dried in vacuo. Yield: 3.35 g of the title compound, 84% of theory, as beige crystals, (HPLC: 91% area).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07456283B2 |
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| 출처 데이터셋 | uspto-grants-2008_11 |
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| ORD ID | ord-fea1ab82bcff4fe4be20be0b5a11e35d |
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| 출처 메모 | uspto-grants-2008_11 |
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