참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | (2,2-Diethoxyethyl)dimethylamine | HCID 77163 | — |
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | Diethyl 2-(4-(3,4-dichlorophenylamino)pyrido[3,4-d]pyrimidin-6-ylamino)-2-oxoethylphosphonate | HCID 86668936 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Dimethylacetamide | HCID 31374 | — |
| 용매 | Dichloromethane methanol | HCID 21226129 | — |
| 생성물 | HCID 51037657 | HCID 51037657 | 95% |
반응 단계
To a stirred mixture of 2,2-diethoxy-N,N-dimethylethanamine (2.08 g, 12.9 mmol) and water (2.2 mL) at room temperature and under a nitrogen atmosphere was added an aq. 37% HCl (2.16 mL, 25.7 mmol). After addition the mixture was stirred at 40° C. (bath) for 20 h. It was cooled to 0° C. (bath). This is called solution A. KOH (1.84 g, 32.9 mmol) was dissolved in water (10 mL) at room temperature under a nitrogen atmosphere. It was cooled to 0° C. (bath). This is called solution B. To a stirred heterogeneous mixture of compound 231 (2.49 g, 5.14 mmol) and THF (10 mL) at room temperature and under a nitrogen atmosphere was added minimum amount of DMA (5.5 mL) to give a homogeneous solution. LiCl (218 mg, 5.14 mmol) was added and stirred at 0° C. (bath) for 15 min. The cold solution B was added and stirred at 0° C. for 2 min. Then the cold solution A was added and the final reaction mixture was continued to stir at 0° C. under a nitrogen atmosphere. The reaction was monitored by TLC (DCM-MeOH=10:1). After 15 min it was found ca. 20% of compound 231 left. More KOH (0.40 g, 7.14 mmol) was added as a solid. After stirred further for 15 min. it was poured into water (300 mL). Petroleum ether (300 mL) was added and stirred at room temperature for 15 min. Petroleum ether layer was decanted. More petroleum ether (300 mL) was added and stirred for 15 min. The solid was collected by suction filtration; washed with water (4×30 mL); dried under reduced pressure over silica gel/KOH to give (2E)-N-[4-(3,4-dichloroanilino)pyrido[3,4-d]-pyrimidin-6-yl]-4-(dimethylamino)-2-butenamide (4) (2.03 g, 95%) as a beige solid, mp 161-164° C.; HPLC: 98.6% pure; 1N NMR δ [(CD3)2SO] 10.92 (s, 1H), 10.36 (s, 1H), 9.09-8.95 (m, 2H), 8.67 (br s, 1 H), 8.27 (br s, 1 H), 7.92 (br d, J=7.8 Hz, 1H), 7.65 (d, J=8.8, 1H), 6.88 (dt, J=15.4, 6.0 Hz, 1H), 6.52 (br d, J=15.4 Hz, 1H), 3.09 (dd, J=6.0, 1.2 Hz, 2H), 2.19 (s, 6H). Anal. Calcd for C19H18Cl2N6O.1.2H2O: C, 51.99; H, 4.69; N, 19.15. Found C, 51.93; H, 4.59; N, 19.15.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09101632B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-8bbc8dac73c44541bd6920e6c67538ac |
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| 출처 메모 | uspto-grants-2015_08 |
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