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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952530Generated: November 3, 2026

indium(III)bromide → Benzyl 4-(6-(5-bromo-4-(2-ethoxy-2-oxoethyl)thiophene-2-carbonyl)-1H-indol-2-yl)benzoate

https://huagongshe.com/reaction/1952530

Reaction equation

Participants

RoleNameHCIDCharge
Reactantindium(III)bromideHCID 167051—
ReactantBenzyl 4-((2-amino-4-(5-bromo-4-(2-ethoxy-2-oxoethyl)thiophene-2-carbonyl)phenyl)ethynyl)benzoateHCID 67496516—
SolventTolueneHCID 1140—
ProductBenzyl 4-(6-(5-bromo-4-(2-ethoxy-2-oxoethyl)thiophene-2-carbonyl)-1H-indol-2-yl)benzoateHCID 6749655676%

Reaction Steps

To a 25 mL flask containing freshly distilled toluene (10 mL) was added benzyl 4-((2-amino-4-(5-bromo-4-(2-ethoxy-2-oxoethyl)thiophene-2-carbonyl)phenyl)ethynyl)benzoate (100 mg, 0.17 mmol) and indium tribromide (24 mg, 0.06 mmol) under N2. The resulting mixture was refluxed for one hour. The solvent was removed in vacuo. MPLC purification (Hex:EtOAc/4:1) of the crude product gave 4 as a yellow solid (76 mg, 76%). 1H NMR (400 MHz, CDCl3) δ 9.50 (brs, 1H), 8.16 (d, J=8.0 Hz, 2H), 8.02 (s, 1H), 7.82 (d, J=8.4 Hz, 2H), 7.65 (q, J=8.4 Hz, 2H), 7.55 (s, 1H), 7.48-7.34 (m, 5H), 6.98 (s, 1H), 5.39 (s, 2H), 4.19 (q, J=7.2 Hz, 2H), 3.64 (s, 2H), and 1.28 (t, J=7.2 Hz, 3H); 13C NMR (100 MHz, CDCl3) δ 187.53, 170.09, 166.24, 143.98, 140.75, 136.91, 136.16, 136.07, 135.92, 135.09, 132.96, 131.53, 130.74, 129.74, 128.90, 128.59, 128.53, 125.56, 122.10, 121.94, 120.81, 113.74, 101.86, 67.14, 61.66, 35.37, and 14.43.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404728B2
Source datasetuspto-grants-2013_03
ORD IDord-e7f6452ae63b4d6e9167eb96063718f3
Source noteuspto-grants-2013_03