Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 59490939 | HCID 59490939 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59490928 | HCID 59490928 | 80% |
Reaction Steps
Compound B4 was diluted with tetrahydrofuran (3 mL) and to the resulting solution was added 1M aqueous lithium hydroxide (2 mL, excess). The reaction was heated to 70° C. and allowed to stir at this temperature for 14 hours. The reaction was then acidified using 1M HCl, and extracted several times with ethyl acetate. The organic layer was collected and concentrated in vacuo to provide 1-(2-Fluoro-benzyl)-3-(2-methoxy-pyridin-3-yl)-5-methyl-1H-pyrrolo[3,2-b]pyridine-2-carboxylic acid B5 (0.2 g, 80% yield). MS: 392.16 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404845B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-a64bdb1c732c4ce5a34194bf812ea673 |
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| Source note | uspto-grants-2013_03 |
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