Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 59771802 | HCID 59771802 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11664058 | HCID 11664058 | — |
Reaction Steps
(R)-Methyl 3-(1-((R)-7-((4-Fluoropiperidin-1-yl)methyl)-3,4-dihydro-2H-chromen-4-yl)-1H-1,2,3-triazol-4-yl)-2-(4-methylphenylsulfonamido)propanoate (130. mg, 0.228 mmol), 1N LiOH (0.3 mL, 0.3 mmol) in 4 mL MeOH was stirred for 14 h at RT. The reaction mixture was then stirred at 55° C. for 24 h. The reaction mixture was cooled, concentrated and neutralized with 1N HCl. A precipitate formed that was filtered and washed with ether to afford the title compound. MS (m/z): 558.4 (m+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414134B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-7ea0807abb9641adb197386e23641d04 |
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| Source note | uspto-grants-2008_08 |
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