Hydrochloric Acid → HCID 178426488, compound
Reaction equation
C(OC(=O)[NH:7][C@H:8]1[CH2:13][CH2:12][C@@H:11]([NH:14][C:15]2[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][N:16]=2)[CH2:10][CH2:9]1)(C)(C)C.Cl.O1CCOCC1>>[CH3:21][C:18]1[CH:19]=[CH:20][C:15]([NH:14][C@H:11]2[CH2:12][CH2:13][C@@H:8]([NH2:7])[CH2:9][CH2:10]2)=[N:16][CH:17]=1Participants
4
Procedure
To a round bottomed flask was added tert-butyl(cis-4-((5-methylpyridin-2-yl)amino)cyclohexyl)carbamate (0.2795 g, 0.915 mmol) and hydrogen chloride, 4.0M solution in 1,4-dioxane (1.144 ml, 4.58 mmol, Sigma-Aldrich Chemical Company, Inc.) to stir at room temperature for 6 h. Solvent was evaporated in vacuo to provide the title compound, which was carried on without further work up. LCMS showed product peak at 0.357 min (m+1=206.0).
Workup
- customSolvent was evaporated in vacuo
Sources & evidence
- ORD record
- ord-0e908e39c0584045837da2c29aaaeca2
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09174992B2
Reaction notes
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