Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 59314110 | HCID 59314110 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 59314105 | HCID 59314105 | 140.4% |
Reaction Steps
A 100 mL flask containing 2-[(2-ethoxy-pyridine-3-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester ([313], 340 mg, 0.96 mmol) is charged with 1,4-dioxane (4 mL) and MeOH (4 mL). A stirring bar is added and stirring is initiated. After dissolution, water (2 mL) is added followed by the LiOH monohydrate (102 mg, 2.42 mmol). After 13 days, tlc analysis (silica, 10% MeOH/DCM) indicates that the starting material is completely consumed. The contents of the flask are diluted with iPrOH (30 mL). Dowex Highly Acidic Ion Exchange Resin (2 g) is added. The reaction flask is capped and allowed to stir at ambient temperature. After 18 h, additional iPrOH (35 mL) is added to the reaction flask. The contents of the reaction flask are filtered through a pad of Celite and concentrated under reduced pressure by pumping to constant weight to yield 0.44 g of white solid. This material is dissolved in a mixture of DCM (10 mL) and iPrOH (3 mL). Celite (15 g) is added to the flask. The solvent is removed under reduced pressure. The remaining material is transferred to a 40 mL plastic syringe that is fitted with a fritted disk. The syringe is fitted onto an ISCO Companion which had a 40 g column (silica). The following gradient is applied. 1% IPrOH/DCM for 4 column volumes. Then a linear gradient to 50% iPrOH/DCM over 10 column volumes. Hold at 50% iPrOH/DCM for 2 Column Volumes. 14 mL fractions are collected. Fractions 39-41 are combined and evaporated by pumping to constant weight to yield white solid (0.28 g, 89%).
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-c1e9fd4273b845e281e9cbdb7d06d74c |
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| Source note | uspto-grants-2013_10 |
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