Ammonium Hydroxide → HCID 10448672, compound
Reaction equation
C[O:2][C:3](=O)[CH2:4][C:5]([NH:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][C:17]=2[F:23])=[CH:10][CH:9]=1)=[O:6].[OH-].[NH4+:26]>>[F:23][C:17]1[CH:18]=[C:19]([F:22])[CH:20]=[CH:21][C:16]=1[CH2:15][O:14][C:11]1[CH:12]=[CH:13][C:8]([NH:7][C:5](=[O:6])[CH2:4][C:3]([NH2:26])=[O:2])=[CH:9][CH:10]=1Participants
3
Procedure
Prepared in analogy to example 3 from N-[4-(2,4-difluoro-benzyloxy)-phenyl]-malonamic acid methyl ester and ammonium hydroxide. Yield=49%. Colorless solid. MS: m/e=321.1 (M++H).
Sources & evidence
- ORD record
- ord-29fc35af7a1a44a29c2d2a4d19e285f6
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07053245B2
Reaction notes
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