Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Boc-N-methylethylenediamine | HCID 2756424 | — |
| Reactant | 3-Bromo-5-chloropyrazolo(1,5-a)pyrimidine | HCID 45480507 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86697425 | HCID 86697425 | 82% |
Reaction Steps
To 465 mg (2.00 mmol) of 3-bromo-5-chloropyrazolo[1,5-a]pyrimidine was added tert-butyl (2-aminoethyl)(methyl)carbamate (522 mg, 3.00 mmol), 4 mL of isopropanol, and triethylamine (0.56 mL, 4.00 mmol). The resulting mixture is heated at 140° C. for 0.5 hr in the microwave. It was diluted with EtOAc, and washed with water and brine. The organic layer was dried over MgSO4, concentrated and purified on the silica gel column eluting with 20-100% EtOAc/Hex to obtain 607 mg (82%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946415B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-e72bfa5a731b4459807857512c3db50b |
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| Source note | uspto-grants-2015_02 |
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