HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-amino-2H-1,3-benzodiazol-2-one → HCID 178517074, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-amino-2H-1,3-benzodiazol-2-one | HCID 15250547 | — |
| Reactant | 3-(hydroxymethylidene)-1H-indol-2-one | HCID 178418741 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178517074 | HCID 178517074 | 51.3% |
Reaction Steps
A solution of 161 mg (1.00 mMol) of 3-(hydroxymethylene)-1,3-dihydro-2H-indol-2-one, 149 mg (1.00 mMol) of 5-aminobenzimidazolone, and 5 ml of ethanol was heated at 55° C. for 1.5 hr. The resulting solid was isolated by filtration and recrystallized from DMSO/methanol to yield 150 mg (51%) of a yellow solid, 1H NMR (DMSO-d6): δ6.80 (d, J=7.7 Hz, 1H), 6.85-6.98 (m, 4H), 7.00 (s, 1H), 7.54 (d, J=7.4 Hz, 1H), 8.50 (d, J=12.7 Hz, 1H), 10.39 (s, 1H), 10.56 (s, 1H), 10.72 (d, J=12.7 Hz, 1H), 10.74 (s, 1H); APCI-MS m/z291 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06964977B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-4a6d7647c36d4a0fbe05714369f37369 |
| Source note | uspto-grants-2005_11 |