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HRID 511802作成日:2026年10月24日

Hydrochloric Acid → HCID 51037657、化合物

https://huagongshe.com/ja/reaction/511802

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium HydroxideHCID 14797—
反応物(2,2-Diethoxyethyl)dimethylamineHCID 77163—
反応物Lithium ChlorideHCID 433294—
反応物Diethyl 2-(4-(3,4-dichlorophenylamino)pyrido[3,4-d]pyrimidin-6-ylamino)-2-oxoethylphosphonateHCID 86668936—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒DimethylacetamideHCID 31374—
溶媒Dichloromethane methanolHCID 21226129—
生成物HCID 51037657HCID 5103765795%

反応条件

温度40 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09101632B2
出典データセットuspto-grants-2015_08
ORD IDord-8bbc8dac73c44541bd6920e6c67538ac
出典メモuspto-grants-2015_08