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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242848Generated: October 31, 2026

Diisopropylethylamine → HCID 178427375, compound

https://huagongshe.com/reaction/242848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-[3-phenyl-1-(toluene-4-sulfonyl)-1H-indol-2-yl]ethylamineHCID 68157485—
ReactantHCID 178478393HCID 178478393—
Solvent1-ButanolHCID 263—
ProductHCID 178427375HCID 17842737591.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 1-[3-phenyl-1-(toluene-4-sulfonyl)-1H-indol-2-yl]ethylamine (294 mg, 0.753 mmol), 6-chloro-9H-purine (140 mg, 0.903 mmol) and DIPEA (0.20 mL, 1.13 mmol) in n-butanol (1.5 mL) was stirred in a sealed tube for 56 h at 120° C. After cooling to RT, the crude reaction mixture was loaded onto an Isolute® SCX-2 cartridge which was washed with MeOH and the product eluted with 2M NH3/MeOH. The product containing fractions were combined and concentrated under reduced pressure. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-7% 2M NH3/MeOH in DCM) affording N-(1-(3-phenyl-1-tosyl-1H-indol-2-yl)ethyl)-9H-purin-6-amine as a yellow solid (350 mg, 91%). LCMS: RT 3.31 min [M+H]+ 509.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-92e561c1df41424e962dafeeaf7e1966
Source noteuspto-grants-2014_02