Reaction equation
Cl.[NH2:2][CH2:3][CH:4]([NH:15][C:16](=[O:38])[CH2:17][N:18]1[C:22](=[O:23])[N:21]([CH2:24][C@H:25]([OH:30])[C:26]([F:29])([F:28])[F:27])[C:20]([C:31]2[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=2)=[N:19]1)[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[CH:6]=1.[O-:39][C:40]#[N:41].[K+]>CO.O>[C:40]([NH:2][CH2:3][CH:4]([NH:15][C:16](=[O:38])[CH2:17][N:18]1[C:22](=[O:23])[N:21]([CH2:24][C@H:25]([OH:30])[C:26]([F:29])([F:27])[F:28])[C:20]([C:31]2[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=2)=[N:19]1)[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:12])([F:14])[F:13])[CH:6]=1)(=[O:39])[NH2:41]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
Of the compound from Example 11, 266 mg (0.45 mmol) were introduced in 6 ml of methanol/water 1:1 and admixed with potassium cyanate (110 mg, 1.36 mmol) at RT. The mixture was heated at 40° C. for 90 min. Following complete reaction, the mixture was cooled to RT and purified completely by preparative HPLC (Method 10). Drying in an HV gave 232 mg (84% of theory) of the title compound.
Workup
- customreaction
- temperaturethe mixture was cooled to RT
- custompurified completely by preparative HPLC (Method 10)
- customDrying in an HV
Sources & evidence
- ORD record
- ord-42a1b7b0130441aea3295c60497b2674
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08202895B2
Linked notes
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