HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Diazabicyclo(5.4.0)undec-7-ene → dimethylphosphinic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Phosphinic acid, dimethyl-, p-nitrophenyl ester | HCID 166793 | — |
| Reactant | 3-(1H-indol-2-yl)-1H-indazol-5-ol | HCID 136055979 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | dimethylphosphinic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester | HCID 136055994 | 43% |
Reaction Steps
The dimethylphosphinic acid 3-(1H-indol-2-yl)-1H-indazol-5-yl ester compound is prepared according to procedure F using 230 mg of 3-(1H-indol-2-yl)-1H-indazol-5-ol (intermediate B) in solution with 245 mg of dimethylphosphinic acid 4-nitrophenyl ester in 5 ml of dichloromethane (stabilized with amylene) to which 170 μl of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in solution in 2 ml of dichloromethane are added. After stirring for 24 h at ambient temperature, the solvent is evaporated off and the crude is purified by preparative LC/MS. The crystals obtained after concentration of the fractions are washed with ethyl acetate and then with isopropyl ether. 129 mg of expected product are collected. Yield=43%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07491710B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-316e1ee481684e4cba0966f68fcfe0d0 |
| Source note | uspto-grants-2009_02 |