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HRID 20719作成日:2026年10月24日

Trimethyl Phosphate → 5-(4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-2-oxo-2H-chromen-8-yloxy)pentyl dihydrogen phosphate

https://huagongshe.com/ja/reaction/20719

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl PhosphateHCID 10541—
反応物Phosphorus oxychlorideHCID 24813—
反応物4-(3,5-Dichloropyridin-4-ylamino)-8-(5-hydroxypentyloxy)-7-methoxy-2H-chromen-2-oneHCID 24849890—
溶媒WaterHCID 962—
生成物5-(4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-2-oxo-2H-chromen-8-yloxy)pentyl dihydrogen phosphateHCID 59347962—

反応手順

Phosphoryl trichloride (69.4 mg, 0.46 mmol) was added to a solution of 4-(3,5-dichloropyridin-4-ylamino)-8-(5-hydroxypentyloxy)-7-methoxy-2H-chromen-2-one (100 mg, 0.22 mmol, Example 72) and trimethyl phosphate (2 mL). After 1 h at rt, water (0.5 mL) was added, and the reaction was stirred for an additional 2 h. The solution was directly purified by reverse-phase HPLC to give 5-(4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-2-oxo-2H-chromen-8-yloxy)pentyl dihydrogen phosphate: 1H NMR (400 MHz, DMSO-d6): δ 10.88 (br, 2H), 9.52 (s, 1H), 8.81 (s, 2H), 7.94 (d, 1H), 7.20 (d, 1H), 4.64 (s, 1H), 3.98 (t, 2H), 3.92 (s, 3H), 3.82 (m, 2H), 1.70 (m, 2H), 1.62 (m, 2H), 1.51 (m, 2H); MS (ESI): 518.9.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745646B2
出典データセットuspto-grants-2010_06
ORD IDord-5441e3d0b83b413cb59a7570be04cb50
出典メモuspto-grants-2010_06