Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520342Generated: November 1, 2026

Methyl Acrylate → HCID 178499682, compound

https://huagongshe.com/reaction/1520342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178517517HCID 178517517—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 178499682HCID 17849968249%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 6-iodo-2-(pyridin-3-yl) quinazolin-4-ol (synthesized as described in Scheme 1 and 4, substituting 5-iodo-2-nitrobenzoic acid for 2-nitro-5-propoxy-benzoic acid) (3.00 g, 8.6 mmol, 1.0 eq.), Pd(OAc)2 (48 mg, 0.21 mmol, 0.025 eq.) and PPh3 (113 mg, 0.43 mmol, 0.05 eq.) in DMF (8 mL) was added methyl acrylate (3.22 g, 25.8 mmol, 3.0 eq.) and DIPEA (1.22 g, 9.46 mmol, 1.1 eq.) under Ar atmosphere. The mixture was stirred at 110° C. overnight. After cooling, the mixture was filtered and the solid was washed with ethyl acetate three times to afford 1.30 g of xxxvi-a as green solid (yield 49%). LCMS m/z=308.0 (M+1) (Method B) (retention time=1.41 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073890B2
Source datasetuspto-grants-2015_07
ORD IDord-2fa2c089d9604857b540902ac096d94d
Source noteuspto-grants-2015_07