Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423358Generated: October 29, 2026

Iodoethane → Ethyl 3-(3-chloro-5-{5-[3-chloro-4-(ethyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1-yl)propanoate

https://huagongshe.com/reaction/423358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-{3-chloro-5-[5-(3-chloro-4-hydroxyphenyl)-1,2,4-oxadiazol-3-yl]-1H-indol-1-yl}propanoateHCID 136146071—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-(3-chloro-5-{5-[3-chloro-4-(ethyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1-yl)propanoateHCID 59318429—

Reaction Conditions

Temperature80 °C

Reaction Steps

To ethyl 3-{3-chloro-5-[5-(3-chloro-4-hydroxyphenyl)-1,2,4-oxadiazol-3-yl]-1H-indol-1-yl}propanoate (D108) (180 mg, 0.40 mmol) and K2CO3 (138 mg, 1.0 mmol) in dry DMF (3 ml) was added ethyl iodide (78 mg, 0.50 mmol) and the mixture heated at 80° C. with stirring for 30 minutes. Cooled mixture and added EtOAc (50 ml). Washed with water (3×40 ml) and dried over MgSO4. Evaporated off the solvent and crystallised from ethanol to yield the title compound as 110 mg of white solid. δH (400 MHz, d6-DMSO) 1.10 (3H, t), 1.42 (3H, t), 2.90 (2H, t), 4.02 (2H, q), 4.27 (2H, q), 4.49 (2H, t), 7.40 (1H, d), 7.74 (1H, s), 7.80 (1H, d), 7.95 (1H, dd), 8.16 (1H, dd), 8.21-8.22 (2H, m). MS (ES) C23H2135Cl2N3O4 requires 473; found 474 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101775B2
Source datasetuspto-grants-2012_01
ORD IDord-7e7a437694fe40fcb220802b4a1cdcae
Source noteuspto-grants-2012_01