HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726054Generated: November 4, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → methylphenylphosphinic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester
https://huagongshe.com/reaction/1726054
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-Nitrophenyl P-methyl-P-phenylphosphinate | HCID 114796 | — |
| Reactant | 3-(1H-indol-2-yl)-1H-indazol-5-ol | HCID 136055979 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methylphenylphosphinic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester | HCID 136055967 | — |
Reaction Steps
A solution of 497 mg of 50%-pure methylphenylphosphinic acid 4-nitrophenyl ester in 8 ml of dichloromethane is stirred at ambient temperature. A suspension of 403 mg of 3-(1H-indol-2-yl)-1H-indazol-5-ol and 268 μl of 1,8-diazabicyclo[5.4.0]undec-7-ene in 12 ml of dichloromethane is added dropwise. The reaction medium is stirred at ambient temperature overnight and then evaporated to dryness under reduced pressure in a rotary evaporator. The reaction crude is purified by flash chromatography on a cartridge of 50 g of silica 15-35 μm. 300 mg of methylphenylphosphinic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester are collected and recrystallized from ethyl acetate to obtain 220 mg of methylphenylphosphinic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl 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-c60ecef54d794526965a742e90793216 |
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| Source note | uspto-grants-2009_02 |
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