HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919618Generated: October 30, 2026
Diisopropylethylamine → HCID 86706478, compound
https://huagongshe.com/reaction/919618
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Chloro-7-(p-toluenesulfonyl)-7H-pyrrolo[2,3-d]pyrimidine | HCID 44228967 | — |
| Reactant | HCID 69676423 | HCID 69676423 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | HCID 86706478 | HCID 86706478 | 36.5% |
Reaction Steps
To a solution of 1-(3-amino-4-methylpiperidin-1-yl)-2-(3,5-dichlorophenylamino)ethanone (180 mg, 0.56 mmol) and 4-chloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine (192 mg, 0.62 mmol) in DMF (5 mL), was added DIEA (0.15 mL, 0.85 mmol) and the reaction mixture was stirred at 60° C. overnight. The reaction mixture was cooled to rt and diluted with EtOAc/water (1:2, 120 mL). The EtOAc layer was separated, dried over Na2SO4 and evaporated in vacuo to give a residue that was purified by column chromatography (silica gel, gradient EtOAc in hexanes) to afford the titled intermediate (120 mg, 35%). LC-MS: m/z [M+1]=587.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273028B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-b5e42205bb364854be0f5ff35eafa99e |
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| Source note | uspto-grants-2016_03 |
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