Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 87479192 | HCID 87479192 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68506786 | HCID 68506786 | — |
Reaction Steps
A solution of 7M NH3 in methanol (35 mL) is added to methanesulfonic acid 2-hydroxy-2-{4-[5-(2-isopropylamino-6-methyl-pyrimidin-4-yl)-[1,2,4]oxadiazol-3-yl]-phenyl}-ethyl ester (606 mg, 1.40 mmol, synthesis described for Example 143). The reaction mixture is stirred at 65° C. for 18 h and is then evaporated to give 293 mg of rac-2-amino-1-{4-[5-(2-isopropylamino-6-methyl-pyrimidin-4-yl)-[1,2,4]oxadiazol-3-yl]-phenyl}-ethanol as a yellow oil; LC-MS: tR=0.73 min; [M+H]+=355.06.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299086B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-e42d80c3cbc0492b84e468e2fe458adc |
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| Source note | uspto-grants-2012_10 |
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