Hydrochloric Acid → HCID 18445312, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:20]=[CH:19][C:18]([C:21](=[O:23])[NH2:22])=[CH:17][N:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:24]>O1CCCC1>[ClH:24].[NH:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:20]=[CH:19][C:18]([C:21]([NH2:22])=[O:23])=[CH:17][N:16]=2)[CH2:10][CH2:9]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Combine 4-(5-carbamoyl-pyridin-2-yloxy)-piperidine-1-carboxylic acid tert-butyl ester (1559 mg, 4.85 mmol) in tetrahydrofuran (25 mL) with hydrochloric acid (4.0 M in dioxane, 15 mL). Stir the resulting reaction mixture for 48 h. Filter the white precipitate washing with EtOAc (10 mL). Redissolve the white solid in methanol and concentrate to provide the title compound (1195 mg, 89%).
Workup
- customthe resulting reaction mixture for 48 h
- filtrationFilter the white precipitate
- washwashing with EtOAc (10 mL)
- dissolutionRedissolve the white solid in methanol
- concentrationconcentrate
Sources & evidence
- ORD record
- ord-889093af302442f1ad7809225ae6438d
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196100B2
Reaction notes
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