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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918685Generated: October 26, 2026

2-(5-Chloro-1-methyl-1H-indol-3-yl)-ethylamine → N-(2-(5-chloro-1-methyl-1H-indol-3-yl)ethyl)-5-(3-fluorobenzyl)isoxazole-3-carboxamide

https://huagongshe.com/reaction/1918685

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-Chloro-1-methyl-1H-indol-3-yl)-ethylamineHCID 6487610—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant5-(3-Fluorobenzyl)isoxazole-3-carboxylic acidHCID 66832107—
SolventDimethylformamideHCID 6228—
ProductN-(2-(5-chloro-1-methyl-1H-indol-3-yl)ethyl)-5-(3-fluorobenzyl)isoxazole-3-carboxamideHCID 6683183836.8%

Reaction Steps

A solution of 5-(3-fluorobenzyl)isoxazole-3-carboxylic acid (0.057 g; 0.257 mmol), 2-(5-chloro-1-methyl-1H-indol-3-yl)ethanamine (0.060 g; 0.284 mmol), HATU (0.108 g; 0.284 mmol) and N,N-diisoprpylethylamine (0.112 mL; 0.649 mmol) in DMF (3 mL), was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and sodium hydrogen sulfate, the organic layer was washed with sodium carbonate, brine, dried and concentrated under reduced pressure. The crude mixture was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.039 g (36%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-010a5c94071241259dab10184cf0b092
Source noteuspto-grants-2013_12