HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252795Generated: November 2, 2026
Potassium Carbonate → HCID 59645279, compound
https://huagongshe.com/reaction/2252795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 6-[4-(Chloromethyl)phenyl]-N-((R)-1-phenylethyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine | HCID 59756711 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59645279 | HCID 59645279 | — |
Reaction Steps
A mixture of 1.6 g (4 mmol) [6-(4-chloromethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-((R)-1-phenyl-ethyl)-amine (for the preparation see Example 9, Step 9.3 of WO 03/013541 A1) in 50 ml DMF is treated with 1.56 g (8.4 mmol) N—BOC-piperazine and 2.76 g (20 mmol) anhydrous potassium carbonate and the mixture heated to 65° C. for 1 hour. The reaction mixture is cooled and the inorganic salts removed by filtration (Hyflo Super Cel®; Fluka, Buchs, Switzerland). The DMF is evaporated under reduced pressure and the residue purified through flash chromatography using first dichloromethane/ethanol 95:5 and then dichloromethane/ethanol 9:1. The title compound is obtained as a solid; m.p. 244-246° C.; MS-ES+: (M+H)+=513; TLC Rf(dichloromethane/ethanol 9:1) 0.46.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07323469B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-e71f314ab44b4139ae93591b9524df4d |
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| Source note | uspto-grants-2008_01 |
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