Hydrochloric Acid → HCID 66782075, compound
Reaction equation
C(OC(=O)[NH:7][CH2:8][CH2:9][CH2:10][N:11]1[C:19]([O:20]C)=[N:18][C:17]2[C:12]1=[N:13][C:14]([O:23][CH2:24][CH2:25][CH2:26][CH3:27])=[N:15][C:16]=2[NH2:22])(C)(C)C.Cl>C(OCC)C.CCCC(C)C.O1CCOCC1>[NH2:22][C:16]1[N:15]=[C:14]([O:23][CH2:24][CH2:25][CH2:26][CH3:27])[N:13]=[C:12]2[C:17]=1[NH:18][C:19](=[O:20])[N:11]2[CH2:10][CH2:9][CH2:8][NH2:7]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The product from step (i) (1.1 g) was dissolved in methanol/DCM (1/1, 40 ml). 4N—HCl in dioxane (10 ml) was added and the mixture stirred at rt for 20 h. The resultant was concentrated under reduced pressure, which afforded the subtitle compound. Yield 0.9 g.
Workup
- concentrationThe resultant was concentrated under reduced pressure, which
Sources & evidence
- ORD record
- ord-68a4b9e0fbf94b55ab3cabb364b98ebb
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08138172B2
Reaction notes
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