tert-butyl N-(4-chlorophenyl)carbamate → (2-Amino-5-chloro-phenyl)-(2,4-difluoro-phenyl)-methanone

HRID 513123

反応式

HRID 513123 の反応式
[Cl:1][C:2]1[CH:15]=[CH:14][C:5]([NH:6]C(OC(C)(C)C)=O)=[CH:4][CH:3]=1.[F:16][C:17]1[CH:25]=[C:24]([F:26])[CH:23]=[CH:22][C:18]=1[C:19](Cl)=[O:20]>>[NH2:6][C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:15][C:14]=1[C:19]([C:18]1[CH:22]=[CH:23][C:24]([F:26])=[CH:25][C:17]=1[F:16])=[O:20]

参加物

3

反応物 2

HCID 546372tert-butyl N-(4-chlorophenyl)carbamateHCID 5880812,4-Difluorobenzoyl chloride

生成物 1

HCID 64423774(2-Amino-5-chloro-phenyl)-(2,4-difluoro-phenyl)-methanone収率 20%

実験手順

In a manner similar to that described above for compound 1aa, 4-Chloro-N-Boc-aniline and 2,4-difluoro-benzoyl chloride were converted to 1w (20% yield) MS m/z=268 (M+H).

出典と根拠

ORDレコード
ord-58cdec6ff740401b8563bb9cd855a2ab
出典データセット
uspto-grants-2015_08
特許番号
US09102678B2

関連ノート

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