Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67342733 | HCID 67342733 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67344796 | HCID 67344796 | 75.2% |
Reaction Steps
To a suspension of 0.480 g (1.18 mmol) of 5′-chloro-3′-(3-chloro-benzoylamino)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-carboxylic acid methyl ester in a 1:1 mixture of water:methanol (10 mL) is added 1.0 mL (2.5 mmol) of sodium hydroxide as a 10% aqueous solution. The mixture is stirred at room temperature overnight then concentrated under reduced pressure to remove volatile organics. The pH is adjusted to approximately pH 5 by the addition of a 2N solution of hydrochloric acid causing a solid to precipitate from solution. The material is collected by filtration, washed with water, and dried on the filter pad to provide 0.35 g (75%) of 5′-chloro-3′-(3-chloro-benzoylamino)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-carboxylic acid as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952004B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-0697394031394487a73e0c23b0031a42 |
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| Source note | uspto-grants-2015_02 |
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