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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382476Generated: October 31, 2026

2-Ethylbutyric acid → HCID 69907473, compound

https://huagongshe.com/reaction/382476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethylbutyric acidHCID 6915—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Ethylbutyryl chlorideHCID 75954—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86757539HCID 86757539—
SolventPyridineHCID 1049—
ProductHCID 69907473HCID 6990747371.2%

Reaction Steps

tert-Butyl (R)-N-[2-[7-carbamoyl-1-(3-hydroxy-propyl)-1H-indol-5-yl]-1-methylethyl]-N-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]carbamate (2.00 g) was dissolved in dry pyridine (3 ml), and 2-ethylbutyryl chloride (0.54 g) prepared from 2-ethylbutyric acid and oxalyl chloride was added to the solution. After the mixture was stirred overnight at room temperature, a saturated aqueous sodium bicarbonate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous sodium bicarbonate solution and brine subsequently, and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo, and the residue was purified by column chromatography on silica gel (eluent:hexane/ethyl acetate=2/1) to give white amorphous (R)-3-[5-[2-[N-(tert-butoxycarbonyl)-N-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]amino]propyl]-7-carbamoyl-1H-indol-1-yl]propyl 2-ethylbutyrate (1.66 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310086B1
Source datasetuspto-grants-2001_10
ORD IDord-2158b88281ae4f99976e5109611b41c7
Source noteuspto-grants-2001_10