Cesium carbonate → HCID 86690930, compound
Reaction equation
Br[CH2:2][C:3]1[CH:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15]([F:18])([F:17])[F:16])[N:6]=[CH:5][N:4]=1.[Cl:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]2[N:27]([CH2:32][C@H:33]([OH:38])[C:34]([F:37])([F:36])[F:35])[C:28](=[O:31])[NH:29][N:30]=2)=[CH:22][CH:21]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>C(#N)C>[Cl:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]2[N:27]([CH2:32][C@H:33]([OH:38])[C:34]([F:36])([F:37])[F:35])[C:28](=[O:31])[N:29]([CH2:2][C:3]3[CH:8]=[C:7]([C:9]4[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=4[C:15]([F:18])([F:17])[F:16])[N:6]=[CH:5][N:4]=3)[N:30]=2)=[CH:22][CH:21]=1Participants
5
Conditions
- Temperature
- 60 °C
Procedure
37 mg (0.12 mmol) of the compound from Example 82A were dissolved in 2 ml of acetonitrile, and 39 mg (0.13 mmol) of the compound from Example 5A and 57 mg (0.18 mmol) of cesium carbonate were added. The mixture was stirred at 60° C. for 2.5 h. After cooling to RT, the solid was filtered off and rinsed with a little acetonitrile. The filtrate was concentrated under reduced pressure and directly purified chromatographically [Method 19]. The product obtained was subjected to a further chromatographic purification on silica gel (mobile phase: cyclohexane/ethyl acetate 4:1, then 3:2). This gave 28 mg (41% of theory) of the target compound.
Workup
- temperatureAfter cooling to RT
- filtrationthe solid was filtered off
- washrinsed with a little acetonitrile
- concentrationThe filtrate was concentrated under reduced pressure
- customdirectly purified chromatographically [Method 19]
- customThe product obtained
- customwas subjected to a further chromatographic purification on silica gel (mobile phase
Sources & evidence
- ORD record
- ord-e99a21b0a0634327a0d32f3cece8c4b5
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09187466B2
Reaction notes
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