Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746444Generated: October 30, 2026

Ammonium Hydroxide → HCID 11234212, compound

https://huagongshe.com/reaction/746444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 11236119HCID 11236119—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11234212HCID 1123421242%

Reaction Steps

A solution of N-(3,5-dichloropyrid-4-yl)-4-methoxy-8-acetamido-dibenzo[b,d]furan-1-carboxamide (60 mg) (Example 4) and 25-28% aqueous ammonium hydroxide (3 ml) in THF (35 ml) was hydrogenated at 50 psi using 10% Pd/C (60 mg) for 24 h at room temperature. The reaction was filtered through celite and the filtrate was concentrated. The residue was dissolved in DCM, washed with water and brine, dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography using 2-10% methanol in DCM as eluent to obtain 21 mg (42%) of N-(pyrid-4-yl)-4-methoxy-8-acetamido-dibenzo[b,d]furan-1-carboxamide as white solid. mp: 267-268° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393846B2
Source datasetuspto-grants-2008_07
ORD IDord-ca781bd3141644c6892378d065954128
Source noteuspto-grants-2008_07