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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852610Generated: October 25, 2026

Sodium Carbonate → methyl 3-(1-methylethyl)-7-nitro-1H-indole-5-carboxylate

https://huagongshe.com/reaction/852610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 3-bromo-4-[(3-methyl-2-buten-1-yl)(trifluoroacetyl)amino]-5-nitrobenzoateHCID 86602879—
ReactantHCID 178526064HCID 178526064—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Productmethyl 3-(1-methylethyl)-7-nitro-1H-indole-5-carboxylateHCID 69358662135.1%

Reaction Steps

To a solution of ethyl 3-bromo-4-[(3-methyl-2-buten-1-yl)(trifluoroacetyl)amino]-5-nitrobenzoate (D215) (12.9 g, 28.5 mmol, 1 equiv) in DMF (130 ml) were added HCOONa (1.94 g, 28.5 mmol, 1 equiv), Na2CO3 (7.54 g, 71.2 mmol, 2.5 equiv), Bu4NCI (8.7 g, 31.3 mmol, 1.1 equiv) and palladium (II) acetate (320 mg, 1.42 mmol, 0.05 equiv) and the resulting mixture was stirred under nitrogen for 1 h then cooled to room temperature and concentrated in vacuo. The residue was partitioned between AcOEt and H2O and the two layers were separated. The insoluble material in the aqueous phase was filtered off through a pad of celite and the aqueous layer extracted twice with AcOEt. The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo to give methyl 3-(1-methylethyl)-7-nitro-1H-indole-5-carboxylate (D218) (10.1 g, 128%) as a black solid which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-1296be22aad6463db62bdfedbffd8138
Source noteuspto-grants-2007_08