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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240027Generated: November 2, 2026

Isopropylamine → HCID 16071255, compound

https://huagongshe.com/reaction/2240027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantHCID 58812060HCID 58812060—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16071255HCID 1607125557.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of toluene-4-sulfonic acid 2-[1-methyl-3-(naphthalene-1-sulfonyl)-1H-indazol-5-yloxy]-ethyl ester (0.433 g, 0.807 mmol) and isopropylamine (1.0 mL, 12 mmol) in THF (10 mL) was stirred at 80° C. in a sealed tube for 15 hours. Additional isopropylamine (1.0 mL, 12 mmol) was added, and the reaction mixture was stirred at 80° C. for 21 hours. It was allowed to cool to room temperature, and partitioned in ethyl acetate and aqueous sodium bicarbonate. The organic phase was washed with water and brine. It was dried with anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography using 0.25% ammonium hydroxide/2.5% methanol in chloroform. Drying at 63° C. in vacuo for 30 minutes yielded isopropyl-{2-[1-methyl-3-(naphthalene-1-sulfonyl)-1H-indazol -5-yloxy]-ethyl}-amine as a yellow semi-solid 0.198 g, 57.9%). This was dissolved in chloroform, and ethereal hydrochloride was added. The precipitate was filtered and dried at 85° C. in vacuo for 13 hours to give the hydrochloride as an off-white solid (0.180 g): MP: 274-6° C. (dec).; Mass Spectrum (+EI, [M+H]+) m/z 424.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723329B2
Source datasetuspto-grants-2010_05
ORD IDord-023811b499c24f3f948da9679a111389
Source noteuspto-grants-2010_05