HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423030Generated: October 27, 2026
Diisopropylethylamine → ethyl 4-(aminomethyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylate
https://huagongshe.com/reaction/423030
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro- | HCID 5356682 | — |
| Reactant | Ethyl 4-(aminomethyl)piperidine-4-carboxylate | HCID 57750280 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | ethyl 4-(aminomethyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylate | HCID 57750365 | 95% |
Reaction Steps
N-Ethyldiisopropylamine (3.70 ml, 21.26 mmol) was added to ethyl 4-(aminomethyl)piperidine-4-carboxylate (Intermediate 9) (3.3 g, 17.7 mmol) and 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (2.72 g, 17.72 mmol) in DMA (35 ml). The resulting solution was stirred at 60° C. for 18 hours. The crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and pure fractions were evaporated to dryness to afford ethyl 4-(aminomethyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylate (5.08 g, 95%) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08101623B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-989ee9f4f8244844abadc793b4fa3f24 |
|---|
| Source note | uspto-grants-2012_01 |
|---|