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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527166Generated: October 26, 2026

Water → 1-Carbamoyl-6-ethyl-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1527166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium ChloriteHCID 23668197—
Reactant6-Ethyl-3-formyl-indole-1-carboxylic acid amideHCID 86673790—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
Product1-Carbamoyl-6-ethyl-1H-indole-3-carboxylic acidHCID 68283406—

Reaction Steps

6-Ethyl-3-formyl-indole-1-carboxylic acid amide (720 mg, 3.33 mmol) was dissolved in a mixture of THF (60 mL) and t-butanol (18 mL). 2-methyl-2-butene (2 M solution in THF, 66.6 mL, 133 mmol) was added, followed by a water (16 mL) solution of NaClO2 (80%, 3.76 g, 33.3 mmol) and NaH2PO4 (3.20 g, 26.6 mmol). The resulting solution was stirred at RT for 4 h and THF was concentrated. EtOAc was added and the layers separated. The aqueous layer was acidified by addition of HCl 1N and extracted twice with EtOAc. The combined organic extracts were dried (Na2SO4), filtered and concentrated. The crude residue was purified by flash column chromatography on silica gel (eluent: c-hexane to EtOAc to CH2Cl2/MeOH 8:2) to give the desired compound. tR (HPLC conditions a): 2.17 min. 1H-NMR (400 MHz, CDCl3): δ (ppm): 12.9 (m, 1H), 8.81 (s, 1H), 8.66 (bs, 1H), 8.23 (d, 1H),), 8.09 (m, 2H), 7.70 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-57ffc23845c1456fbb3d33b16fe19551
Source noteuspto-grants-2015_07