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HRID 272572作成日:2026年10月26日

Diethyl chlorophosphate → (3-Oxo-2,3-dihydro-7-oxa-1,2-diaza-benzo[de]anthracen-10-ylmethyl)-phosphoramidic acid diethyl ester

https://huagongshe.com/reaction/272572

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl chlorophosphateHCID 13139—
反応物10-(Aminomethyl)[1]benzopyrano[4,3,2-de]phthalazin-3(2H)-oneHCID 11196355—
溶媒DimethylformamideHCID 6228—
生成物(3-Oxo-2,3-dihydro-7-oxa-1,2-diaza-benzo[de]anthracen-10-ylmethyl)-phosphoramidic acid diethyl esterHCID 1135013750%

反応手順

To a solution of compound 49 (0.5 mmol) in anhydrous DMF (20 mL) was added diethyl chlorophosphate (1.5 mmol). After 3 hours solution was concentrated in vacuo, and 50 mL of water was added. The aqueous layer was extracted with 30 mL of EtOAc twice. Organic layers were combined and washed with 30 mL of brine. Organic layer was dried with MgSO4. Solvent was removed to afford a white solid, which was recrystallized in 10% of EtOAc in hexanes to afford a white solid 54 in 50% yield. MS (ES−): 400; Mp: 222.3-224.5° C.; 1H-NMR (CDCl3, 400 MHz): 10.21 (s, 1H), 8.10 (d, J=2.5 Hz, 1H), 8.03 (d, J=7.5 Hz, 1H), 7.79 (t, J=8.0 Hz, 1H), 7.52 (d, J=8.0 Hz, 1H), 7.47 (dd, J=8.5 and 2.0 Hz, 1H), 7.22 (d, J=8.5 Hz, 1H), 4.12 (m, 6H), 1.32 (t, J=6.5 Hz, 6H); Anal. Calcd. for C19H20N3O5P.(0.3H2O): C, 56.10; H, 5.10; N, 10.33. Found: C, 56.00; H, 5.03; N, 10.13.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456178B2
出典データセットuspto-grants-2008_11
ORD IDord-954d85a485854be3b1c49262cb9aed60
出典メモuspto-grants-2008_11