HCID 18538721, compound → 956075-57-3
Reaction equation
[N:1]1([CH2:6][CH:7]2[CH2:12][CH2:11][N:10](C(OC(C)(C)C)=O)[CH2:9][CH2:8]2)[CH:5]=[CH:4][CH:3]=[N:2]1>Cl.O1CCOCC1>[N:1]1([CH2:6][CH:7]2[CH2:8][CH2:9][NH:10][CH2:11][CH2:12]2)[CH:5]=[CH:4][CH:3]=[N:2]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The title compound from Step B above (100 mg, 0.4 mmol) was dissolved in 4 M HCl in dioxane (4.0 mL) and stirred at RT for 1 h. The product was concentrated under reduced pressure and dried under high vacuum to give the title compound (i-28) (59 mg, 95%). ESI-MS calculated for C9H15N3: Exact Mass: 165.13. Found 166.12.
Workup
- concentrationThe product was concentrated under reduced pressure
- customdried under high vacuum
Sources & evidence
- ORD record
- ord-d4978eadc86c46b2a59b06ce4046329c
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08354403B2
Reaction notes
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