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HRID 1956715作成日:2026年10月27日

2,4-Difluorobenzylamine → 3-(2,4-Difluoro-benzylamino)-4-(1,1-dimethyl-propylamino)-cyclobut-3-ene-1,2-dione

https://huagongshe.com/reaction/1956715

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-DifluorobenzylamineHCID 2733244—
反応物3-Ethoxy-4-(1,1-dimethyl-propylamino)-cyclobut-3-ene-1,2-dioneHCID 17819403—
溶媒AcetonitrileHCID 6342—
生成物3-(2,4-Difluoro-benzylamino)-4-(1,1-dimethyl-propylamino)-cyclobut-3-ene-1,2-dioneHCID 10662573—

反応手順

This compound was prepared according to the procedure for Example 59. From 3-ethoxy-4-(1,1 -dimethyl-propylamino)-cyclobut-3-ene- 1,2-dione and 2,4-difluorobenzylamine in acetonitrile. The title compound was obtained, after recrystallization from diethyl ether, as a white solid (80%): mp 242°-244° C.; 1H NMR (DMSO-d6) δ0.82 (t, 3H), 1.30 (s, 6H), 1.68 (q, 2H), 4.76 (d, 2H), 7.09 (m, 1H), 7.27 (m, 1H), 7.50 (m, 2H), 7.80 (m, 1H) ppm; IR (KBr) 3250, 3150, 2970, 1790, 1652, 1580, 1538, 1510 cm-1 ; MS (m/z) 309 ([M+H]+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05780505
出典データセットuspto-grants-1998_07
ORD IDord-b753f3c2598f46c98cd0e6750741f097
出典メモuspto-grants-1998_07