HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44413Generated: October 24, 2026
Triethylamine → N-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine
https://huagongshe.com/en/reaction/44413
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-benzyl-N,4-dimethylpiperidin-3-amine | HCID 9943889 | — |
| Reactant | HCID 178418725 | HCID 178418725 | — |
| Product | N-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine | HCID 12084829 | 50% |
Reaction Steps
A solution of 4-chloropyrrolo[2,3-d]pyrimidine (2.4 grams, 15.9 mmol), prepared by the method of Davoll, J. Am. Chem. Soc., 82, 131 (1960), which is incorporated by reference in its entirety, and the product from Method A (1.7 grams, 7.95 mmol) dissolved in 2 equivalents of triethylamine was heated in a sealed tube at 100° C. for 3 days. Following cooling to room temperature and concentration under reduced pressure, the residue was purified by flash chromatography (silica; 3% methanol in dichloromethane) affording 1.3 grams (50%) of the title compound as a colorless oil. LRMS: 336.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541426B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-90ce4c8ad50f4e4aa7af55ff18e28333 |
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| Source note | uspto-grants-2013_09 |
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