Methyl propiolate → HCID 22258312, compound
Reaction equation
Cl.[CH3:2][C:3]1[N:4]=[C:5]([CH2:9][C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([CH3:18])[CH:13]=2)=[O:11])[NH:6][C:7]=1[CH3:8].C[O-].[Na+].[C:22](OC)(=[O:25])[C:23]#[CH:24]>>[CH3:8][C:7]1[NH:6][C:5]2[N:4]([C:3]=1[CH3:2])[C:22](=[O:25])[CH:23]=[CH:24][C:9]=2[C:10](=[O:11])[C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([CH3:18])[CH:13]=1Participants
4
Procedure
The compound is prepared as described in example 25 with 300 mg (1.13 mmol) of 2-(4,5-Dimethyl-1H-imidazol-2-yl)-1-(3-methylphenyl)ethanone hydrochloride (example XXII), 65 mg (1.20 mmol) of sodium methylate and 95.3 mg (1.13 mmol) methyl propiolate.
Workup
- customThe compound is prepared
Sources & evidence
- ORD record
- ord-1a7b2a4658d94fe7901e120917c753ff
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06984646B2
Reaction notes
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