HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571699Generated: October 30, 2026
Diisopropylethylamine → HCID 67969468, compound
https://huagongshe.com/reaction/571699
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(Boc-amino)piperidine | HCID 4233041 | — |
| Reactant | 7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro- | HCID 5356682 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67969468 | HCID 67969468 | — |
Reaction Steps
To a solution of tert-butyl piperidin-3-ylcarbamate compound (5.0 g, 25 mmol) and 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (3.75 g, 25 mmol) in DMF (50 mL) was added DIEA (4.2 mL, 3.1 g, 25 mmol) and the solution was stirred at 100° C. for 4 h. The reaction mixture was concentrated in vacuo and the residue was purified by column chromatography to give tert-butyl 1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidin-3-ylcarbamate. To a solution of tert-butyl 1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidin-3-ylcarbamate (6.3 g, 20 mmol) in dioxane (50 ml) was added 4.0 N HCl (50 mL, 200 mmol) and stirred at rt. After several hours, the reaction mixture was concentrated in vacuo to give compound 33.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029359B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-aa72c85b17704567a2b004f9fc3287a1 |
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| Source note | uspto-grants-2015_05 |
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