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HRID 1169872作成日:2026年10月27日

Carbon Tetrachloride → Benzenemethanamine, 2,5-dichloro-

https://huagongshe.com/reaction/1169872

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon TetrachlorideHCID 5943—
反応物BenzylamineHCID 7504—
反応物N-bromobutanimideHCID 67184—
反応物2-Chloro-5-iodotolueneHCID 4200996—
反応物Phthalimide potassium saltHCID 24194345—
溶媒DimethylformamideHCID 6228—
生成物Benzenemethanamine, 2,5-dichloro-HCID 457600—
生成物2-Chloro-5-iodobenzylamineHCID 11460882—

反応手順

The various benzylamine derivatives used in this study, when not commercially available, were synthesized by the methods shown in FIG. 5. 2,5-Dichlorobenzylamine 64 and 2-chloro-5-iodobenzylamine 65 were prepared from the corresponding benzyl bromides. Compound 60 was prepared from 2-chloro-5-iodotoluene by bromination with N-bromosuccinimide in CCl4. Wilson et al., J. Med. Chem 1989, 32, 1057-1062. 60 and 61 were treated with potassium phthalimide in N,N-dimethylformamide at 60° C. to obtain compounds 62 and 63 as white solids in 95% yield. Deprotection with hydrazine gave 64 and 65 in 80% yield. Treu et al., Molecules 2002, 7, 743-750.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07825126B2
出典データセットuspto-grants-2010_11
ORD IDord-90cacdc0e5ea44a0be82d06ded280f36
出典メモuspto-grants-2010_11