HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726065Generated: November 1, 2026
Sodium Chloride → phenylphosphonic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester methyl ester
https://huagongshe.com/reaction/1726065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Bis(4-nitrophenyl) P-phenylphosphonate | HCID 170133 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(1H-indol-2-yl)-1H-indazol-5-ol | HCID 136055979 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | phenylphosphonic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester methyl ester | HCID 136055973 | 103% |
Reaction Steps
Phenylphosphonic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester methyl ester is prepared according to procedure F using 230 mg of phenyl-phosphonic acid bis-(4-nitrophenyl) ester in solution in 4 ml of dichloromethane to which is added a solution of 120 mg of 3-(1H-indol-2-yl)-1H-indazol-5-ol and 72 μl of 1,8-diazabicyclo[5.4.0]undec-7-ene in 4 ml of dichloromethane. After stirring for 2 hours at ambient temperature, the medium is treated with 4 times 50 ml of a saturated sodium bicarbonate solution, and then with 2×50 ml of a saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and then concentrated to dryness to obtain 200 mg of crude phenylphosphonic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07491710B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-0f206f75f0264c24a797d5131fdc5427 |
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| Source note | uspto-grants-2009_02 |
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