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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376612Generated: November 1, 2026

Methanol → HCID 10150867, compound

https://huagongshe.com/reaction/2376612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantHCID 69267066HCID 69267066—
Catalystpalladium(II) acetateHCID 167845—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 10150867HCID 1015086727%

Reaction Steps

A mixture of N-(6,7-Methylenedioxycinnolin-4-yl)-N-(n-butyl)-2-iodo-4,5-dimethoxybenzamide (1.0 mmol equiv.), Pd(OAc)2 (0.2 mmol equiv.), P(o-tolyl)3 (0.4 mmol equiv.), and Ag2CO3 (2.0 mmol equiv) was heated to reflux in DMF (30 mL per mmol equiv.) with stirring. The reaction mixture was allowed to cool to room temperature, diluted with CHCl3, and filtered through Celite. The sicciate was extensively washed with 10% CH3OH in CHCl3. The filtrate was concentrated in vacuo and the residue chromatographed on silica gel using chlorofomm:methanol to provide the title compound (123 mg, 0.2 mmol) in 27% yield with a reaction time 90 min; mp 299° C.; IR (KBr) 1654; 1H NMR (CDCl3) δ 1.06 (t, 3H, J=7.4), 1.56 (m, 2H), 2.13 (m, 2H), 4.09 (s, 3H), 4.17 (s, 3H), 4.49 (m, 2H), 6.26 (s, 2H), 7.62 (s, 1H), 7.85 (s, 1H), 7.87 (s, 1H), 8.65 (s, 1H); 13C NMR (CDCl3) δ 13.8, 20.2, 31.1, 48.6, 56.3, 56.6, 98.8, 102.7, 104.2, 106.5, 107.9, 119.7, 149.1, 150.1, 150.9, 151.4, 153.6, 154.2, 162.9; HRMS calcd for C22H21N3O5H, 408.1559; found 408.1543

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468366B2
Source datasetuspto-grants-2008_12
ORD IDord-b74ac29053ea4e40aa22f3b1de6a6c9a
Source noteuspto-grants-2008_12