3-oxo-1,3-dihydroisobenzofuran-1-ylphosphonic acid synthesis
- Product Name:3-oxo-1,3-dihydroisobenzofuran-1-ylphosphonic acid
- CAS Number:61260-15-9
- Molecular formula:C10H11O5P
- Molecular Weight:242.17
Yield:61260-15-9 96%
Reaction Conditions:
Stage #1: dimethyl phosphonate;o-carboxybenzaldehydewith natrium in methanol at 0 - 20; for 6 h;
Stage #2: with Eaton′s Reagent in methanol; for 0.5 h;
Steps:
1.2 Dimethyl (3-oxo-l,3,-dihydroisobenzofuran-l-yl)phosphonate
Dimethylphosphite (0.92 mL, 10.0 mmol) was added dropwise to a solution of sodium (0.58 g, 10.8 mmol) in MeOH (15 mL) at 0°C. To the solution, 2-carboxybenzaldehyde (1.00 g, 6.66 mmol) was added portionwise while stirring. The mixture was gradually warmed to room temperature and stirred for 6 hours. Methanesulfonic acid (0.77 mL, 11.9 mmol) was added dropwise and the mixture was stirred for another 30 minutes. The solution was concentrated in vacuo to produce a white solid, to which water was added (30 mL) and the crude product was extracted into DCM (3 x 30 mL). The organic layer was washed with water (2 x 30 mL), dried with MgS04 and filtered. The filtrate was concentrated in vacuo and washed with EbO (3 x 20 mL), affording Dimethyl-(3-oxo-l,3-dihydrobenzofuran-l- yl)phosphonate (1.54 g, 96%) as a white solid. *H NMR (400 MHz, CD3OD) d = 7.94 (d, J = 7.5 Hz 1H), 7.83 (t, J = 7.5 Hz, 1H), 7.75 (d, J = 7.5 Hz, 1H), 7.68 (t, J = 7.5 Hz, 1H), 6.10 (d, J = 10.8, 1H), 3.91 (d, J = 10.8 Hz, 3H), 3.72 (d, J - 10.8 Hz, 3H). Data is in accordance with known literature; Mp: 90 - 92°C (Menear, K.A., et al. 4-[3-(4-cyclopropanecarbonylpiperazine-l-carbonyl)-4-fluorobenzyl]-2H- phthalazin- l-one: a novel bioavailable inhibitor of poly(ADP-ribose) polymerase- 1. J Med Chem 51, 6581-6591, 2008).
References:
WO2019/186135,2019,A1 Location in patent:Page/Page column 62-63
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