HCID 67972218, compound → HCID 67060710, compound
Reaction equation
[CH:1]1([N:4]2[C:8]([CH:9]3[CH2:14][CH2:13][N:12](C(OC(C)(C)C)=O)[CH2:11][CH2:10]3)=[N:7][N:6]=[N:5]2)[CH2:3][CH2:2]1>Cl.O1CCOCC1>[CH:1]1([N:4]2[C:8]([CH:9]3[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]3)=[N:7][N:6]=[N:5]2)[CH2:3][CH2:2]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The title compound from Step B above (200 mg, 0.68 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 the title compound (i-37) (127 mg, 96%). ESI-MS calculated for C9H15N5: Exact Mass: 193.13. Found 194.14.
Workup
- concentrationThe product was concentrated under reduced pressure
- dry with materialdried under high vacuum to the title compound (i-37) (127 mg, 96%)
Sources & evidence
- ORD record
- ord-0295ce42d1b84493a23b3862506c7628
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08354403B2
Reaction notes
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