Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | L-Valinol | HCID 640993 | — |
| Reactant | 3-Bromo-5-chloropyrazolo(1,5-a)pyrimidine | HCID 45480507 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67034301 | HCID 67034301 | 99% |
Reaction Steps
To a solution of (S)-2-amino-3-methylbutan-1-ol (3.3 g, 32 mmol) in DMF was added 3-bromo-5-chloropyrazolo[1,5-a]pyrimidine (2.5 g, 11 mmol) and N-ethyl-N-isopropylpropan-2-amine (4.2 g, 32 mmol) and the reaction was heated to 100° C. for 4 hours. The reaction mixture was poured into EtOAc and washed with water and brine, dried over magnesium sulfate and concentrated in vacuo to yield (S)-2-(3-bromopyrazolo[1,5-a]pyrimidin-5-ylamino)-3-methylbutan-1-ol (3.2 g, 99%). LCMS (APCI+) m/z 299, 301 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865726B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-87f9a51b3bde4849a87d0898f2594334 |
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| Source note | uspto-grants-2014_10 |
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