Hydrochloric Acid → HCID 90411982, compound
Reaction equation
[F:1][C:2]1[CH:3]=[N:4][C:5]([O:8][CH2:9][CH:10]2[CH2:15][CH:14]3[N:16](C(OC(C)(C)C)=O)[CH:11]2[CH2:12][CH2:13]3)=[N:6][CH:7]=1.Cl>O1CCOCC1.CC(O)C>[F:1][C:2]1[CH:3]=[N:4][C:5]([O:8][CH2:9][CH:10]2[CH2:15][CH:14]3[NH:16][CH:11]2[CH2:12][CH2:13]3)=[N:6][CH:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 40 °C
Procedure
To the title compound from step A (474 mg, 1.5 mmol) in 1,4-dioxane (1.5 mL) was added 6N HCl in iPrOH (1.5 mL). The reaction was heated to 40° C. for 1.5 h and concentrated to give the title compound that was used without further purification in subsequent steps. MS (ESI) mass calcd. for C11H14FN3O, 223.1; m/z found 224.0 [M+H]+.
Workup
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-45e6c8c823da4ba0873d26483468d182
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062078B2
Reaction notes
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