Methyl propiolate → HCID 22258266, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:8](=[O:19])[CH2:9][C:10]2[NH:14][C:13]3[CH2:15][CH2:16][CH2:17][CH2:18][C:12]=3[N:11]=2)[CH:5]=[CH:6][CH:7]=1.C[O-].[Na+].[C:23](OC)(=[O:26])[C:24]#[CH:25]>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:6][CH:7]=1)[C:8]([C:9]1[CH:25]=[CH:24][C:23](=[O:26])[N:14]2[C:13]3[CH2:15][CH2:16][CH2:17][CH2:18][C:12]=3[NH:11][C:10]=12)=[O:19]Participants
4
Procedure
The compound is prepared as described in example 20 with 559.9 mg (2.03 mmol) of 1-(3-Chlorophenyl)-2-(4,5,6,7-tetrahydro-1H-benzimidazol-2-yl)ethanone (example XXXIX), 220.2 mg (4.08 mmol) of sodium methylate and 171.3 mg (2.03 mmol) methyl propiolate.
Workup
- customThe compound is prepared
Sources & evidence
- ORD record
- ord-6cbabfb1e73245baa74b260e88607506
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06984646B2
Reaction notes
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