HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552310Generated: November 1, 2026
Diisopropylethylamine → HCID 67152512, compound
https://huagongshe.com/reaction/552310
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 22281400 | HCID 22281400 | — |
| Reactant | 7-(4-Bromo-2,6-dimethylphenyl)-4-chloro-2,5,6-trimethyl-7H-pyrrolo[2,3-d]pyrimidine | HCID 58281345 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67152512 | HCID 67152512 | 78.8% |
Reaction Steps
A suspension of 7-(4-bromo-2,6-dimethyl-phenyl)-4-chloro-2,5,6-trimethyl-7H-pyrrolo[2,3-d]pyrimidine (2.0 g), 3-(piperidin-4-yl)propionitrile (1.4 g) and N,N-diisopropylethylamine (1.4 g) in EtOH (4 mL) was heated at 100° C. in a sealed tube for 11 hours. After cooling to room temperature, the solvent was removed under reduced pressure. The residue was purified with column chromatography (silica gel: Wako gel C200, eluent: hexane:ethyl acetate:CHCl3=8/2/1) to obtain 3-{1-[7-(4-bromo-2,6-dimethyl-phenyl)-2,5,6-trimethyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-piperidin-4-yl}-propionitrile (2.0 g) as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951811B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-fb6f4f8d59ac4bbe865308624aee22f0 |
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| Source note | uspto-grants-2011_05 |
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