HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indazolinone → 3-Oxo-1,3-dihydroindazole-2-carboxylic acid 2-methylbenzylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indazolinone | HCID 81829 | — |
| Reactant | 1-(Isocyanatomethyl)-2-methylbenzene | HCID 2733386 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Oxo-1,3-dihydroindazole-2-carboxylic acid 2-methylbenzylamide | HCID 11448895 | — |
Reaction Steps
105 mg (0.78 mmol) of 1H-indazol-3-ol were reacted in 3 ml of THF with 138.3 mg (0.94 mmol) of 1-isocyanatomethyl-2-methylbenzene to give 3-oxo-1,3-dihydroindazole-2-carboxylic acid 2-methylbenzylamide. 50 mg (178 μmol) of this compound were stirred in 3 ml of pyridine with 40 mg (355 μmol) of triethylamine and 43 mg (266 μmmol) of 4-methylpiperidine-1-carbonyl chloride at room temperature for 7 h. Addition of a further 120 mg of 4-methylpiperidine-1-carbonyl chloride and 100 mg of triethylamine in 3 portions was followed by stirring again for 7 h, concentration and purification by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 48 mg (66%), M+H+: 407.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357698B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-19b3a3fac38d4a5db0d10fd5963d7c8e |
| Source note | uspto-grants-2013_01 |