HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726094Generated: November 2, 2026
Ethanol → phenylphosphonic acid 1H-indazol-5-yl ester methyl ester
https://huagongshe.com/reaction/1726094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | phenylphosphonic acid 1-acetyl-1H-indazol-5-yl ester 4-nitrophenyl ester | HCID 57562494 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | phenylphosphonic acid 1H-indazol-5-yl ester methyl ester | HCID 57562461 | 62% |
Reaction Steps
A solution of 2.4 g of phenylphosphonic acid 1-acetyl-1H-indazol-5-yl ester 4-nitrophenyl ester in 30 ml of dichloromethane stabilized with ethanol is stirred at 20° C. A solution of 3.78 ml of methanol and of 836 mg of 1,8-diazabicyclo[5.4.0]undec-7-ene in 30 ml of dichloromethane is added thereto. The reaction is continued at this temperature overnight. The reaction mixture is evaporated under reduced pressure and the crude compound thus obtained is then purified by chromatography on silica (AIT BP-SUP 20-40 μm, eluent 90/10 dichloromethane/methanol). The fractions containing the expected compound are combined and evaporated under reduced pressure. 980 mg of phenylphosphonic acid 1H-indazol-5-yl ester methyl ester are isolated and characterized.
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-c11e89cb09dc483b98758da4e5ca38e5 |
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| Source note | uspto-grants-2009_02 |
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