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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-{3-chloro-5-[5-(3-chloro-4-hydroxyphenyl)-1,2,4-oxadiazol-3-yl]-1H-indol-1-yl}propanoate | HCID 136146071 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-(3-chloro-5-{5-[3-chloro-4-(ethyloxy)phenyl]-1,2,4-oxadiazol-3-yl}-1H-indol-1-yl)propanoate | HCID 59318429 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101775B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-7e7a437694fe40fcb220802b4a1cdcae |
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| Source note | uspto-grants-2012_01 |
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