HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonic Acid → HCID 58346321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonic Acid | HCID 7371 | — |
| Reactant | 6-(6-chloropyrimidine-4-carbonyl)-4-methyl-3H-benzoxazol-2-one | HCID 58181206 | — |
| Reactant | 5-amino-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-one | HCID 59166722 | — |
| Solvent | 2-Pentanol | HCID 22386 | — |
| Product | HCID 58346321 | HCID 58346321 | — |
Reaction Steps
144 mg (0.500 mmol) 6-(6-chloropyrimidine-4-carbonyl)-4-methyl-3H-benzoxazol-2-one, 126 mg (0.500 mmol) 5-amino-1,3-dihydrospiro[inden-2,3′-pyrrolo[2,3-b]pyridin]-2′(1′H)-one and 16.1 mg (0.100 mmol) benzenesulphonic acid were combined in 5.0 mL 2-pentanol and refluxed for 4 h. The reaction mixture was evaporated down, the residue was triturated with PE, suction filtered and washed with PE. The residue was purified by preparative HPLC, the fractions containing the product were combined and the organic solvent was eliminated i.vac. The aqueous phase was neutralised by the addition of 1N aqueous NaOH solution. The product precipitated as a solid was filtered off, washed with water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450327B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-68ec62dfd40f49a08f223c0874f9c878 |
| Source note | uspto-grants-2013_05 |