113137-33-0 → HCID 69007532, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][CH:16]=1)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([NH2:13])=[CH:9][CH:8]=1.[CH3:17][O:18][C:19](=[O:26])[CH:20]([O:24][CH3:25])[C:21](O)=[O:22]>>[CH3:17][O:18][C:19](=[O:26])[CH:20]([O:24][CH3:25])[C:21]([NH:13][C:10]1[CH:11]=[CH:12][C:7]([O:6][CH2:5][C:4]2[CH:14]=[CH:15][CH:16]=[C:2]([F:1])[CH:3]=2)=[CH:8][CH:9]=1)=[O:22]Participants
3
Procedure
The title compound is prepared in analogy to example 2 from 4-(3-Fluoro-benzyloxy)-phenylamine and 2-methoxy-malonic acid monomethyl ester (Swan et al.; J. Chem. Soc. Perkin Trans. 1; 1985; 1757-1766). Yield=41%. Colorless solid. MS: m/e=348.2 (M++H).
Sources & evidence
- ORD record
- ord-0115cf77f2e94768bd1f341ffcdaf524
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07053245B2
Reaction notes
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