Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 68579853 | HCID 68579853 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68580053 | HCID 68580053 | 44.6% |
Reaction Steps
Lithium hydroxide (2 M, 4 ml) was warmed to 40° C. and a solution of methyl 2-(4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-6-methoxypyrimidine-4-carboxylate (Example 315, 0.30 g, 0.68 mmol) in MeOH was added. The reaction temperature was increased to 60° C. and it was stirred at that temperature for 3 h. The MeOH was removed, the aqueous solution was cooled to 0° C. and then acidified with 1 N HCl. The precipitate was collected by suction filtration and washed with EtOAc to give the title compound (0.13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709503B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-f7e42e56f8bb4f18b2150ca4ddf264b5 |
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| Source note | uspto-grants-2010_05 |
|---|