Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907354Generated: November 3, 2026

Pyridine → HCID 3616760, compound

https://huagongshe.com/reaction/1907354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant1H-indole-6-carboxylic acidHCID 595230—
SolventTetrahydrofuranHCID 8028—
ProductHCID 3616760HCID 3616760107.3%

Reaction Steps

In a round-bottomed flask, 5.0 g of indole-6-carboxylic acid, 3.3 g of N,O-dimethylhydroxylamine hydrochloride, 11.9 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide and 10 ml of pyridine are placed in 150 ml of tetrahydrofuran. The mixture is stirred at ambient temperature for 40 h. The mixture is concentrated, and the residue is taken up in 150 ml of ethyl acetate and 50 ml of water. The organic phase is washed with 50 ml of a 1N solution of sodium hydroxide and 50 ml of a saturated solution of sodium chloride, dried over magnesium sulphate and then concentrated under reduced pressure. 6.8 g of compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598166B2
Source datasetuspto-grants-2013_12
ORD IDord-21266a9bd66a4329ac39c09680c06e98
Source noteuspto-grants-2013_12