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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175715Generated: November 2, 2026

Triethylamine → (Z)-ethyl 2-(6,7-dimethoxy-1-oxo-2,3-dihydroisoquinolin-4(1H)-ylidene)acetate

https://huagongshe.com/reaction/2175715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant(Z)-ethyl 4-(2-iodo-4,5-dimethoxybenzamido)but-2-enoateHCID 70935552—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
Product(Z)-ethyl 2-(6,7-dimethoxy-1-oxo-2,3-dihydroisoquinolin-4(1H)-ylidene)acetateHCID 8667272383.4%

Reaction Steps

A stirred solution of Pd(OAc)2 (16 mg, 0.07 mmol), PPh3 (61 mg, 0.23 mmol), Et3N (0.58 mL, 4.2 mmol) and (Z)-ethyl 4-(2-iodo-4,5-dimethoxybenzamido)but-2-enoate (860 mg, 2.1 mmol) in dry CH3CN (20 mL) was heated at 70° C. overnight under an argon atmosphere. The reaction was allowed to cool to room temperature and then concentrated under reduced pressure. The residue was purified by flash chromatography using DCM/MeOH 100:1 (v:v) as eluent to give (Z)-ethyl 2-(6,7-dimethoxy-1-oxo-2,3-dihydroisoquinolin-4(1H)-ylidene)acetate (510 mg, 83%). LC-MS (ES-API); rt 7.56 min; m/z calculated for C15H17NO5 [M+H]+ 292.1, found 292.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062076B2
Source datasetuspto-grants-2015_06
ORD IDord-ca64e2c803a34e0ca1017c186a7adc40
Source noteuspto-grants-2015_06