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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063386Generated: November 1, 2026

5-amino-2H-1,3-benzodiazol-2-one → HCID 178517074, compound

https://huagongshe.com/reaction/1063386

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-amino-2H-1,3-benzodiazol-2-oneHCID 15250547—
Reactant3-(hydroxymethylidene)-1H-indol-2-oneHCID 178418741—
SolventEthanolHCID 702—
ProductHCID 178517074HCID 17851707451.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964977B2
Source datasetuspto-grants-2005_11
ORD IDord-4a6d7647c36d4a0fbe05714369f37369
Source noteuspto-grants-2005_11