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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868410Generated: November 1, 2026

1-Naphthalenesulfonyl chloride → HCID 11509961, compound

https://huagongshe.com/reaction/1868410

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Naphthalenesulfonyl chlorideHCID 66560—
Reactant1,1,1-trifluoro-3-(1H-indol-3-yl)propan-2-amineHCID 53988436—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
ProductHCID 11509961HCID 11509961—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 100 mg (0.44 mmol) of 2,2,2-trifluoro-1-(1H-indol-3-ylmethyl)ethylamine and 99 mg (0.44 mmol) of 1-naphthylsulfonyl chloride in 4 mL of pyridine was warmed at 70° C. After 3 hours, the mixture was cooled and concentrated to afford a thick oily residue. The residue was diluted with ether and washed twice with 10% aqueous acetic acid and brine, dried over sodium sulfate, decanted and concentrated in vacuo. The crude material was crystallized from ether-hexanes to afford 102 mg (55%) as off white needles, MS: m/z 419.3 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635711B2
Source datasetuspto-grants-2009_12
ORD IDord-15550f1546a94254857e8b16360b8be8
Source noteuspto-grants-2009_12