Cesium carbonate → HCID 44125592, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:9][CH:10]=[C:11]([CH2:13][S:14][C:15]3[N:20]=[C:19]([N:21]([CH3:27])[CH2:22][C:23]([O:25][CH3:26])=[O:24])[C:18]([C:28]#[N:29])=[C:17]([C:30]4[CH:35]=[CH:34][C:33]([O:36][CH2:37][CH2:38][OH:39])=[CH:32][CH:31]=4)[C:16]=3[C:40]#[N:41])[N:12]=2)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>C(#N)C>[NH2:29][C:28]1[C:18]2[C:19](=[N:20][C:15]([S:14][CH2:13][C:11]3[N:12]=[C:8]([C:5]4[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=4)[S:9][CH:10]=3)=[C:16]([C:40]#[N:41])[C:17]=2[C:30]2[CH:31]=[CH:32][C:33]([O:36][CH2:37][CH2:38][OH:39])=[CH:34][CH:35]=2)[N:21]([CH3:27])[C:22]=1[C:23]([O:25][CH3:26])=[O:24]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
21 mg (0.035 mmol) of the compound from Example 21A were initially charged in 0.69 ml of acetonitrile, and 45 mg (0.139 mmol) of cesium carbonate were added. The reaction mixture was stirred at 50° C. for 2 h and then cooled. The solid was filtered off and then washed with acetonitrile. The filtrate was concentrated and the residue was dried under high vacuum.
Workup
- temperaturecooled
- filtrationThe solid was filtered off
- washwashed with acetonitrile
- concentrationThe filtrate was concentrated
- customthe residue was dried under high vacuum
Sources & evidence
- ORD record
- ord-235f0e9498e94a2380db77deac065c7a
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08609686B2
Reaction notes
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