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HRID 963454作成日:2026年10月25日

Benzenemethanamine, 3,4-dichloro- → 3-tert-Butylamino-4-(3,4-dichlorobenzylamino)-cyclobut-3-ene-1,2-dione

https://huagongshe.com/reaction/963454

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenemethanamine, 3,4-dichloro-HCID 1608—
反応物3-Butoxy-4-tert-butylamino-cyclobut-3-ene-1,2-dioneHCID 17819389—
溶媒TetrahydrofuranHCID 8028—
生成物3-tert-Butylamino-4-(3,4-dichlorobenzylamino)-cyclobut-3-ene-1,2-dioneHCID 1908242142%

反応手順

A solution of 3-butoxy-4-tert-butylamino-cyclobut-3-ene-1,2-dione (1.13 g, 5 mmol, Example 10) and 3,4-dichlorobenzylamine (0.880 g, 5.0 mmol) in tetrahydrofuran (15 mL) was stirred at room temperature for approximately 96 hours. The residue isolated after removal of solvent was recrystallized from N,N-dimethylformamide (twice) and from 2-methoxyethanol to provide 0.687 g (42%) of the title compound as a white solid: mp 302°-303° C.; 1H NMR (DMSO-d6) δ 7.77 (m, 1H), 7.65 (d, 1H), 7.62 (d, 1H), 7.55 (s, 1H), 7.33 (m, 1H), 4.71 (d, 2H), 1.35 (s, 9H) ppm. IR (KBr): 3450, 3230, 1800, 1650 cm-1. MS (m/z) 326/328/330 (M+). HPLC indicates a major component (>99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05763474
出典データセットuspto-grants-1998_06
ORD IDord-a66be46551a941f9a89f754a0a312f09
出典メモuspto-grants-1998_06