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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775454Generated: November 3, 2026

Methylamine → HCID 72948199, compound

https://huagongshe.com/reaction/1775454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTetrahydrofuranHCID 8028—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 118071469HCID 118071469—
SolventTriethylamineHCID 8471—
ProductHCID 72948199HCID 7294819980.4%

Reaction Steps

To 3-(2-aminoethyl)-5-methoxy-N-methyl-1H-indole-2-carboxamide hydrochloride (167 mg) were added tetrahydrofuran (2.00 mL), triethylamine (0.246 mL), and 1,1′-carbonyldiimidazole (143 mg), followed by stirring at room temperature for 15 minutes. Then, methylamine (2 M tetrahydrofuran solution, 1.77 mL) was added thereto, followed by warming to 50° C. and stirring for 1 hour. The reaction mixture was cooled to room temperature, silica gel was added thereto, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform:methanol=100:0 to 20:1) to obtain 5-methoxy-N-methyl-3-{2-[(methylcarbamoyl)amino]ethyl}-1H-indole-2-carboxamide (144 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260445B2
Source datasetuspto-grants-2016_02
ORD IDord-53903977de544c4cb0db3fd0fc632a2c
Source noteuspto-grants-2016_02