Hydrochloric Acid → HCID 68999288, compound
Reaction equation
C[O:2][C:3](=[O:30])[C:4]1[CH:9]=[CH:8][C:7](/[CH:10]=[CH:11]/[C:12]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[NH:14][N:13]=2)=[C:6]([NH:21][C:22]([C:24]2[S:25][CH:26]=[CH:27][C:28]=2[CH3:29])=[O:23])[CH:5]=1.[OH-].[Na+].Cl>CO>[NH:14]1[C:15]2[C:20](=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:12](/[CH:11]=[CH:10]/[C:7]2[CH:8]=[CH:9][C:4]([C:3]([OH:30])=[O:2])=[CH:5][C:6]=2[NH:21][C:22]([C:24]2[S:25][CH:26]=[CH:27][C:28]=2[CH3:29])=[O:23])=[N:13]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
Compound 97 (740 mg, 1.77 mmol) was dissolved in methanol (5.00 mL) and the solution was added with 2 mol/L aqueous sodium hydroxide solution (5.00 mL), followed by stirring at 40° C. for 1 hour. The reaction mixture was acidified by hydrochloric acid (6 mol/L) and the precipitated crystal was collected by filtration to obtain Compound 98 (603 mg, 85%).
Workup
- filtrationthe precipitated crystal was collected by filtration
Sources & evidence
- ORD record
- ord-851b0ff55e3a4414ab2e260928babec8
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07605272B2
Reaction notes
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