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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394920Generated: November 3, 2026

Dimethylformamide → HCID 10449607, compound

https://huagongshe.com/reaction/1394920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHCID 10318130HCID 10318130—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 10449607HCID 10449607—

Reaction Steps

A deoxygenated solution of 4-(5-bromo-2-fluorophenyl)-N,N-dimethyl-2-phenyl-2,5-dihydro-1H-pyrrole-1-carboxamide (2-11, 50 mg, 0.13 mmol, 1 equiv), zinc cyanide (10 mg, 0.85 mmol, 0.66 equiv), tris(dibenzylideneacetone)-dipalladium (12 mg, 0.013 mmol, 0.10 equiv), and 1,1′-bis(diphenylphosphino)-ferrocene (17 mg, 0.031 mmol, 0.24 equiv) in DMF (3 mL) was heated at 110° C. for 3 hours. The reaction mixture was partitioned between brine (50 mL) and ethyl acetate (50 mL). The organic layer was dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography (CH2Cl2 initially, grading to 10% EtOAc in CH2Cl2) to provide 4-(2-fluoro-5-isocyanophenyl)-N,N-dimethyl-2-phenyl-2,5-dihydro-1H-pyrrole-1-carboxamide (13-1) as a pale yellow solid. 1H NMR (500 MHz, CDCl3) δ 7.62 (dd, 1H, j=6.8, 2.0 Hz), 7.59 (m, 1H), 7.33 (m, 4H), 7.26 (m, 1H), 7.22 (dd, 1H, J=10.7, 8.8 Hz), 6.49 (br s, 1H), 6.16 (m, 1H), 4.89 (ddd, 1H, J=13.7, 5.6, 2.0 Hz), 4.55 (d, 1H, J=13.7 Hz), 2.89 (s, 6H). LRMS m/z (M+H) 336.05 found, 336.14 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348440B2
Source datasetuspto-grants-2008_03
ORD IDord-33b71bf71177419884e2cd396ceb416a
Source noteuspto-grants-2008_03