Methyl propiolate → HCID 22258282, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:19])[CH2:9][C:10]1[NH:14][C:13]2[CH2:15][CH2:16][CH2:17][CH2:18][C:12]=2[N:11]=1.C[O-].[Na+].[C:23](OC)(=[O:26])[C:24]#[CH:25]>>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=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 1450 mg (5.90 mmol) of 1-(2-Methylphenyl)-2-(4,5,6,7-tetrahydro-1H-benzimidazol-2-yl)ethanone (example XXXX), 637.2 mg (11.80 mmol) of sodium methylate and 495.8 mg (5.90 mmol) methyl propiolate.
Workup
- customThe compound is prepared
Sources & evidence
- ORD record
- ord-00618767615043ceadbe1ec6ab627d51
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06984646B2
Reaction notes
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