Hydrochloric Acid → HCID 86657590, compound
Reaction equation
[O:1]1[C:9]2[C:4](=[N:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]1[C:10]1([NH2:13])[CH2:12][CH2:11]1.[ClH:14]>O1CCOCC1>[ClH:14].[ClH:14].[O:1]1[C:9]2[C:4](=[N:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]1[C:10]1([NH2:13])[CH2:11][CH2:12]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The Boc-protected 1-(1-oxazolo[4,5-b]pyridin-2-yl-cyclopropylamine (0.044 g, 0.160 mmol) was dissolved in 1,4-dioxane (0.5 mL) and to this solution was added 4N HCl in dioxane (2.50 mL, 10.9 mmol). The solution was stirred for 2 h. A ppt formed and the volatiles were removed in vacuo to afford 1-(1-oxazolo[4,5-b]pyridin-2-yl-cyclopropylamine dihydrochloride as a tan solid (0.023 g, 69%).
Workup
- customA ppt formed
- customthe volatiles were removed in vacuo
Sources & evidence
- ORD record
- ord-13382f0f4d104fc0af798953b8b1f5c6
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08552205B2
Reaction notes
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