N-Methyl-N-[(3R)-pyrrolidin-3-yl]acetamide → HCID 58203783, compound
Reaction equation
[NH:1]1[CH:5]=[C:4]([C:6]2[CH:22]=[CH:21][C:9]3[C:10]4[N:11]=[C:12]([C:18](O)=[O:19])[S:13][C:14]=4[CH2:15][CH2:16][O:17][C:8]=3[CH:7]=2)[CH:3]=[N:2]1.[CH3:23][N:24]([C@@H:28]1[CH2:32][CH2:31][NH:30][CH2:29]1)[C:25](=[O:27])[CH3:26]>>[CH3:23][N:24]([C@@H:28]1[CH2:32][CH2:31][N:30]([C:18]([C:12]2[S:13][C:14]3[CH2:15][CH2:16][O:17][C:8]4[CH:7]=[C:6]([C:4]5[CH:3]=[N:2][NH:1][CH:5]=5)[CH:22]=[CH:21][C:9]=4[C:10]=3[N:11]=2)=[O:19])[CH2:29]1)[C:25](=[O:27])[CH3:26]Participants
3
Procedure
Following the procedure for 103, 8-(1H-Pyrazol-4-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid (50.0 mg, 0.2 mmol) was reacted with (R)—N-methyl-N-(pyrrolidin-3-yl)acetamide (1.2 equiv) to give 180 (24.3 mg, M+1 438.1)
Sources & evidence
- ORD record
- ord-5ae6f88f98e145c581acd72f37efb423
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08673952B2
Reaction notes
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