2-Nitroimidazole → HCID 11020015, compound
Reaction equation
[N+:1]([C:4]1[NH:5][CH:6]=[CH:7][N:8]=1)([O-:3])=[O:2].C(=O)([O-])[O-].[K+].[K+].[CH2:15]([C@@H:17]1[O:19][CH2:18]1)[Cl:16]>>[Cl:16][CH2:15][C@H:17]([OH:19])[CH2:18][N:5]1[CH:6]=[CH:7][N:8]=[C:4]1[N+:1]([O-:3])=[O:2]Participants
4
Procedure
Alternatively, a mixture of 0.42 g (3.7 mmole) of 2-nitroimidazole, 85 mg (0.62 mole) of anhydrous potassium carbonate, and 5 mL of (R)-(-)-epichlorohydrin is refluxed for 10 minutes then filtered while hot. The filtrate is concentrated and cooled to give a solid. Crystallization from ethanol and further processing as above gives 0.56 g of the product.
Workup
- temperatureis refluxed for 10 minutes
- filtrationthen filtered while hot
- concentrationThe filtrate is concentrated
- temperaturecooled
- customto give a solid
- customCrystallization from ethanol and further processing as
Sources & evidence
- ORD record
- ord-4345f8e20f2f4d4da573bbf41597bd7b
- Source dataset
- uspto-grants-1996_01
- Patent number
- US05481000
Reaction notes
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