Itaconic acid → HCID 21920019, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([NH2:17])[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=1.[C:18]([OH:26])(=[O:25])[C:19]([CH2:21][C:22](O)=[O:23])=[CH2:20]>>[F:1][C:2]1[CH:3]=[C:4]([N:17]2[C:22](=[O:23])[CH2:21][CH:19]([C:18]([OH:26])=[O:25])[CH2:20]2)[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=1Participants
3
Procedure
The title compound is prepared in analogy to Example 1a) from 3-fluoro-4-(3-fluoro-benzyloxy)-phenylamine and itaconic acid. Yield: 86% of a colorless solid. MS: m/e=346.1 (M−H).
Sources & evidence
- ORD record
- ord-19ff538f96d84be7a17c6fea603bea0b
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07037935B2
Reaction notes
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