Hydrochloric Acid → HCID 90412405, compound
Reaction equation
[CH3:1][C:2]1[N:7]=C(C#N)[C:5]([N:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)=[CH:4][CH:3]=1.[OH-:15].[K+].Cl.[CH3:18][CH2:19][OH:20]>>[CH3:1][C:2]1[N:7]=[C:18]([C:19]([OH:15])=[O:20])[C:5]([N:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)=[CH:4][CH:3]=1Participants
5
Conditions
- Temperature
- 90 °C
Procedure
To the title compound of Step A (162 mg, 0.9 mmol) in EtOH (2.6 mL) was added 4M KOH (650 μL, 2.6 mmol). The reaction was then heated at 90° C. for 18 h. Additional 4M KOH (1.5 mL, 6 mmol) was added and heating continued overnight. The reaction was then cooled to rt, acidified with 1N HCl (aq), concentrated and used without further purification in the next step.
Workup
- temperatureheating continued overnight
- temperatureThe reaction was then cooled to rt
- concentrationconcentrated
- customused without further purification in the next step
Sources & evidence
- ORD record
- ord-abfe6e8f2f544fa1b1f986d7ac74ca02
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062078B2
Reaction notes
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