HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242848Generated: October 31, 2026
Diisopropylethylamine → HCID 178427375, compound
https://huagongshe.com/reaction/242848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-[3-phenyl-1-(toluene-4-sulfonyl)-1H-indol-2-yl]ethylamine | HCID 68157485 | — |
| Reactant | HCID 178478393 | HCID 178478393 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 178427375 | HCID 178427375 | 91.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653089B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-92e561c1df41424e962dafeeaf7e1966 |
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| Source note | uspto-grants-2014_02 |
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