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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571699Generated: October 30, 2026

Diisopropylethylamine → HCID 67969468, compound

https://huagongshe.com/reaction/571699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Boc-amino)piperidineHCID 4233041—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
SolventDimethylformamideHCID 6228—
ProductHCID 67969468HCID 67969468—

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029359B2
Source datasetuspto-grants-2015_05
ORD IDord-aa72c85b17704567a2b004f9fc3287a1
Source noteuspto-grants-2015_05