HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189774Generated: October 26, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 5-[3-(1H-indazol-5-yl)-1,2,4-oxadiazol-5-yl]-2-[(1-methylethyl)oxy]benzonitrile
https://huagongshe.com/reaction/2189774
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | RP-101124 | HCID 21956832 | — |
| Reactant | HCID 178513242 | HCID 178513242 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[3-(1H-indazol-5-yl)-1,2,4-oxadiazol-5-yl]-2-[(1-methylethyl)oxy]benzonitrile | HCID 53247367 | 32% |
Reaction Steps
3-Cyano-4-[(1-methylethyl)oxy]benzoic acid (can be prepared as described in WO2005/58848) (1.52 g), EDAC (2.14 g) and HOBt (1.51 g) were dissolved in DMF (30 ml) and then stirred for 5 minutes. N-hydroxy-1H-indazole-5-carboximidamide (D2) (1.3 g) was added and the reaction was heated to 80° C. for 6 hours and left to cool overnight. The solvent was removed in vacuo and the crude was partitioned between EtOAc and aq. sodium bicarbonate. The organic layer was separated, dried and evaporated to dryness in vacuo. The resulting solid was triturated with ether and ethyl acetate, washed with methanol and ether to give the title compound (816 mg) as a pink solid. MS (ES): C19H15N5O2 requires 345; found (MH+) 346
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324254B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-bdf82a35c1e9443aa23e76e20dc27041 |
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| Source note | uspto-grants-2012_12 |
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