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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069481Generated: October 30, 2026

Triethylamine → HCID 59729574, compound

https://huagongshe.com/reaction/2069481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2,4-Dibenzyloxy-5-isopropyl-benzoic acidHCID 59167879—
Reactant1,3-Dimethyl-1H-indol-5-amineHCID 59550993—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59729574HCID 5972957495.3%

Reaction Steps

2,4-Dibenzyloxy-5-isopropylbenzoic acid (5.64 g, 15.0 mmol, 1.00 equiv.) in 80 mL dichloromethane at room temperature was treated with oxalyl chloride (2.00 g, 15.75 mmol, 1.05 equiv.) and catalytic amount of DMF (0.1 mL) for 1 hour. Solvent and excess (COCl)2 were removed on rotary evaporator. The residue was dissolved in 100 mL dichloromethane, and treated with 1,3-dimethyl-5-aminoindole (2.40 g, 15.0 mmol, 1.00 equiv.) and triethylamine (2.28 g, 22.5 mmol, 1.50 equiv.) at 0° C. for one hour. Normal aqueous workup and removal of solvent gave a light brown solid that was washed with ether to yield 2,4-dibenzyloxy-5-isopropyl-N-(1-methyl-1H-indol-5-yl)-benzamide (A) as off-white solid (7.20 g, 14.3 mmol, 95%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299107B2
Source datasetuspto-grants-2012_10
ORD IDord-fa25afa9a2f6493aa48e8c7c6b5ed013
Source noteuspto-grants-2012_10