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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206334Generated: October 26, 2026

Acetic Acid → tert-butyl 4-(3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-2-oxo-2H-pyrano[2,3-b]pyridin-7-yl)-1,4-diazepane-1-carboxylate

https://huagongshe.com/reaction/2206334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidineHCID 8082—
ReactantEthyl 2-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)acetateHCID 89657132—
ReactantTert-butyl 4-(5-formyl-6-hydroxypyridin-2-yl)-1,4-diazepane-1-carboxylateHCID 178452079—
SolventEthanolHCID 702—
Producttert-butyl 4-(3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-2-oxo-2H-pyrano[2,3-b]pyridin-7-yl)-1,4-diazepane-1-carboxylateHCID 89793976—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of tert-butyl 4-(5-formyl-6-hydroxypyridin-2-yl)-1,4-diazepane-1-carboxylate (225 mg, 0.7 mmol) in 3 mL of EtOH were treated with piperidine (119.2 mg, 1.4 mmol), acetic acid (252 mg, 4.2 mmol) and ethyl 2-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)acetate (196 mg, 0.84 mmol) at room temperature. The reaction mixture was stirred in microwave reactor at 150° C. for 2 hours. The mixture was concentrated, quenched with a saturated NaHCO3 solution and extracted with dichloromethane three times. The combined organic layers were combined and concentrated. The residue was purified on silica gel to provide tert-butyl 4-(3-(6,8-dimethylimidazo[1,2-a]pyrazin-2-yl)-2-oxo-2H-pyrano[2,3-b]pyridin-7-yl)-1,4-diazepane-1-carboxylate after concentration. MS m/z 491 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371336B2
Source datasetuspto-grants-2016_06
ORD IDord-efa7997f74fe47df9e0442ab66b47dcb
Source noteuspto-grants-2016_06