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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544991Generated: October 27, 2026

Hydrochloric Acid → 2-(3,4-Dimethoxy-phenylamino)-10-iodo-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-one

https://huagongshe.com/reaction/544991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-dimethylaminomethylene-7-iodo-3,4-dihydro-1H-benzo[b]azepine-2,5-dioneHCID 66935066—
ReactantN-(3,4-dimethoxyphenyl)guanidineHCID 178492306—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(3,4-Dimethoxy-phenylamino)-10-iodo-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-oneHCID 59851152—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-dimethylaminomethylene-7-iodo-3,4-dihydro-1H-benzo[b]azepine-2,5-dione (v-a) (1.64 g, 4.6 mmol) in 50 mL EtOH was added K2CO3 (1.82 g, 11.04 mmol) and 1-(3,4-dimethoxyphenyl)guanidine (1.31 g, 5.06 mmol), and the reaction was heated to 80° C. for 12 h. The reaction was then cooled to 22° C., diluted with H2O, and treated with 1 M HCl to pH 3. The resulting solid was filtered and washed with H2O, followed by EtOH and Et2O. The crude product was dried in vacuo to give I-26 (1.8 g, 81%): HRMS Calcd. for C20H17IN4O3: 489.0423, Found 489.0431.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935694B2
Source datasetuspto-grants-2011_05
ORD IDord-cf2ff34500a74fa0800c5a95f27584e1
Source noteuspto-grants-2011_05