HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172979Generated: October 31, 2026
Methyl Acrylate → Methyl 3-(5-(3-(3-chloro-4-isopropoxyphenyl)-1,2,4-oxadiazol-5-yl)isoindolin-2-yl)propanoate
https://huagongshe.com/reaction/1172979
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | 3-(3-Chloro-4-isopropoxyphenyl)-5-(isoindolin-5-yl)-1,2,4-oxadiazole | HCID 59556558 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-(5-(3-(3-chloro-4-isopropoxyphenyl)-1,2,4-oxadiazol-5-yl)isoindolin-2-yl)propanoate | HCID 59556616 | 104% |
Reaction Steps
3-(3-chloro-4-isopropoxyphenyl)-5-(isoindolin-5-yl)-1,2,4-oxadiazole (16.7 mg, 0.047 mmol) was added to a 2 mL microwave vial equipped with a stirring bar. Methyl acrylate (8.45 μL, 0.094 mmol), and methanol (1.0 mL) were added, the vial capped, and the reaction heated to 90° C. for 20 min under microwave irradiation (300 W). After 20 minutes, another aliquot of methyl acrylate (8.45 μL, 0.094 mmol) was added, the vial was re-sealed, and heated to 110° C. for 40 min under microwave irradiation (300 W). Reaction was then concentrated and dried under vacuum overnight to give crude methyl 3-(5-(3-(3-chloro-4-isopropoxyphenyl)-1,2,4-oxadiazol-5-yl)isoindolin-2-yl)propanoate as a yellow oil (21.6 mg, 104%). The product was used without further purification. LCMS (Table 1, Method c) Rt=2.85 min, m/z 442.45 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834039B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-22c710985a0844488372d8246ac8466f |
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| Source note | uspto-grants-2010_11 |
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