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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404089Generated: October 30, 2026

Diisopropylethylamine → ethyl 2-(1-acetyl-5-bromo-7-fluoro-4-methoxy-1H-indol-3-yl)acetate

https://huagongshe.com/reaction/1404089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(Z)-ethyl 4-(N-(2,4-dibromo-6-fluoro-3-methoxyphenyl)acetamido)but-2-enoateHCID 86654327—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Productethyl 2-(1-acetyl-5-bromo-7-fluoro-4-methoxy-1H-indol-3-yl)acetateHCID 6692706779.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To the solution of 8-7 (20 g, 44.0 mmol) in anhydrous DMF (250 mL) was added Pd(OAc)2 (2.0 g, 8.8 mmol), Bu4NBr (14.3 g, 44.0 mmol) and DIPEA (14.2 g, 110 mmol) under N2. The mixture was stirred at 80° C. for 3 h. TLC showed that the reaction was completed. The mixture was poured into ice water and extracted with ethyl acetate (150 mL×3). The organic layers were combined and were concentrated in vacuo. The residue was purified by flash chromatography (Silica-gel, petroleum ether/ethyl acetate=10:1) to afford 8-8 (13.0 g, 79%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912220B2
Source datasetuspto-grants-2014_12
ORD IDord-d372ba9c457242758dd574ed08edbc0c
Source noteuspto-grants-2014_12