Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 59314092 | HCID 59314092 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 25159358 | HCID 25159358 | 94% |
Reaction Steps
A 100 mL round bottom flask which contains 2-{[5-chloro-2-(isopropyl-methyl-amino)-pyridine-3-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester (351, 270 mg, 0.58 mmol) is charged with 1,4-dioxane (3 mL) and MeOH (3 mL). A stirring bar is added and stirring is initiated. After dissolution, water (1.5 mL) is added followed by the LiOH (62 mg, 1.48 mmol). After 18 h, tlc analysis (silica, 50% EtOAc/heptanes) indicates that the starting material is completely consumed. Amberlyst highly acidic exchange resin (0.5 g) is added to the reaction vial. The reaction is capped and allowed to stir at ambient temperature. After 20 h, the contents of the flask are filtered through a pad of Celite. The solvent is removed from the filtrate. The residue is reconstituted with iPrOH/toluene (20+20 mL) and the solvent is removed. This process is repeated 1 time. Pumping to constant weight provides white solid (0.21 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569535B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-20806c2af4cd49618cd2ae8fe3c3b932 |
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| Source note | uspto-grants-2013_10 |
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