Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 7-Nitroindole | HCID 23396 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86668736 | HCID 86668736 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178526401 | HCID 178526401 | — |
Reaction Steps
7-Nitro indole (1 eq.) and oxalyl dichloride (10 eq.) were mixed in ether or CH2Cl2. The reaction was stirred for 24 hours and 2-(7-nitro-1H-indol-3-yl)-2-oxoacetyl chloride precipitated from solution. Filtration offered yellow solid which was dried under vacuum and used in Step 2 without purification. Step 2: iPr2NEt (1-10 eq.) was added into a solution of 2-(7-nitro-1H-indol-3-yl)-2-oxoacetyl chloride from Step 1 and amine (1 eq.) in THF, dioxane or CH2Cl2. The reaction was stirred at room temperature for 24 hours, before being quenched with NaHCO3 (equal volume to THF, dioxane or CH2Cl2 used). The aqueous phase was extracted with EtOAc (3× equal volume to THF, dioxane or CH2Cl2 used). The combined organic phase was dried over MgSO4, filtered and concentrated under vacuum to give a crude product, nitro indole 2-oxoacetyl amide, which was used without purification in the Step 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450361B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-1f58176336c544b181cc92e2d2297faf |
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| Source note | uspto-grants-2013_05 |
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