Aniline → 3-(4-methoxyphenyl)-4-phenyl-5-methyl-4H-1,2,4-triazole

HRID 542871

反応式

[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.P(Cl)(Cl)Cl.[CH3:12][O:13][C:14]1[CH:26]=[CH:25][C:17]([C:18]([NH:20][NH:21][C:22](=O)[CH3:23])=O)=[CH:16][CH:15]=1>ClC1C=CC=CC=1Cl>[CH3:12][O:13][C:14]1[CH:26]=[CH:25][C:17]([C:18]2[N:1]([C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[C:22]([CH3:23])=[N:21][N:20]=2)=[CH:16][CH:15]=1

参加物

実験手順

Using the procedure of Step B in Example 1, 26.3 ml of aniline, 150 ml of o-dichlorobenzene, 4.65 ml of phosphorus trichloride and 10 g of N-(4-methoxybenzoyl)-N'-acetyl-hydrazine [prepared by process of J. Org., Vol. 19 (1954), p. 194-201] were reacted to obtain 7.1 g of 3-(4-methoxyphenyl)-4-phenyl-5-methyl-4H-1,2,4-triazole melting at 140°-141° C.

後処理

customwere reacted

出典と根拠

ORDレコード: ord-37d150b3944448f189500d67a146a3b8
出典データセット: uspto-grants-1987_04
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US04659729

反応式

参加物

反応物 3

生成物 1

試薬・触媒・溶媒 1

実験手順

後処理

出典と根拠

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