Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 86608279 | HCID 86608279 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86608278 | HCID 86608278 | 86% |
Reaction Steps
Lithium hydroxide (2 M, 4 ml) was warmed to 40° C. and a solution of methyl 6-(4-{[(4-bromo-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-2-chloropyrimidine-4-carboxylate (Example 73, 0.180 g, 0.394 mmol) in MeOH was added. The reaction was stirred at 40° C. for 30 mins. The MeOH was removed and the aqueous solution was cooled to 0° C. and it was acidified with 6 M HCl. The acidic solution was extracted with EtOAc, dried over MgSO4 and concentrated to give pink solid (0.15 g, 86%). An analytical sample was purified by reversed phase HPLC (acetonitrile/water (0.1% TFA), 20-95%).
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-9fd0ffa539784f75853be7828df09a00 |
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| Source note | uspto-grants-2010_05 |
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