5-(2-fluorophenyl)furan-2-carbonyl Chloride → HCID 70941517, compound
Reaction equation
CCN(C1C=C[C:9]2[CH:12]=[C:13](/[CH:17]=[N:18]\[NH:19][C:20]3[N:25]=CC=CC=3)C([O:16][C:8]=2C=1)=O)CC.[S:26]([C:30]1[S:34][C:33]([C:35]2[CH:36]=[C:37]([CH:41]=[CH:42][CH:43]=2)[C:38]([OH:40])=O)=[CH:32][CH:31]=1)(=[O:29])(=[O:28])[NH2:27].FC1C=CC=CC=1C1[O:55]C(C(Cl)=O)=CC=1>>[O:16]1[CH:8]=[CH:9][CH:12]=[C:13]1[C:17]1[O:55][C:20]([NH:25][C:38]([C:37]2[CH:41]=[CH:42][CH:43]=[C:35]([C:33]3[S:34][C:30]([S:26](=[O:28])(=[O:29])[NH2:27])=[CH:31][CH:32]=3)[CH:36]=2)=[O:40])=[N:19][N:18]=1Participants
4
Procedure
The title compound was synthesized in accordance with the synthesis method of compound Ic-2 described below, using an acid chloride which can be prepared from 3-(5-sulfamoyl-2-thienyl)benzoic acid described in Reference Example 2 by a routine method instead of 5-(2-fluorophenyl)-2-furancarbonyl chloride.
Sources & evidence
- ORD record
- ord-4e734fb40b1c4e56ac0bf202a24128b0
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08796320B2
Reaction notes
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