Imidazole → HCID 54471508, compound
Reaction equation
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[H-].[Na+].[Cl:8][C:9]1[CH:34]=[C:33]([Cl:35])[CH:32]=[CH:31][C:10]=1[CH2:11][O:12][C@H:13]1[O:18][C@@H:17]([CH2:19]OS(C2C=CC(C)=CC=2)(=O)=O)[CH2:16][CH2:15][CH2:14]1>CN(C)C=O>[Cl:8][C:9]1[CH:34]=[C:33]([Cl:35])[CH:32]=[CH:31][C:10]=1[CH2:11][O:12][C@H:13]1[O:18][C@@H:17]([CH2:19][N:1]2[CH:5]=[CH:4][N:3]=[CH:2]2)[CH2:16][CH2:15][CH2:14]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
As in Example 1(b), 16 mg of imidazole, 10 mg of 55% sodium hydride and 70 mg of cis-6-(2,4-dichlorobenzyloxy)-2-tosyloxymethyltetrahydropyran were reacted in dimethylformamide, to give 37 mg of the title compound in the form of a colourless oil.
Sources & evidence
- ORD record
- ord-6d510b5e615f4deca004a9d2a812b55a
- Source dataset
- uspto-grants-1983_12
- Patent number
- US04421758
Reaction notes
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