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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097666Generated: October 30, 2026

7-Nitroindole → HCID 178526401, compound

https://huagongshe.com/reaction/2097666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-NitroindoleHCID 23396—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86668736HCID 86668736—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178526401HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450361B2
Source datasetuspto-grants-2013_05
ORD IDord-1f58176336c544b181cc92e2d2297faf
Source noteuspto-grants-2013_05