Sodium Azide → 4,5-Dihydro-7-(3,4-dimethoxyphenyl)-4-methyl-5-(2,4,6-trimethylphenylimino)tetrazolo[1,5-a]pyrimidine

HRID 4333

反応式

HRID 4333 の反応式
Cl[C:2]1[N:7]([CH3:8])[C:6](=[N:9][C:10]2[C:15]([CH3:16])=[CH:14][C:13]([CH3:17])=[CH:12][C:11]=2[CH3:18])[CH:5]=[C:4]([C:19]2[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[C:21]([O:27][CH3:28])[CH:20]=2)[N:3]=1.[N-:29]=[N+:30]=[N-:31].[Na+]>CO.O>[CH3:28][O:27][C:21]1[CH:20]=[C:19]([C:4]2[N:3]3[N:29]=[N:30][N:31]=[C:2]3[N:7]([CH3:8])[C:6](=[N:9][C:10]3[C:15]([CH3:16])=[CH:14][C:13]([CH3:17])=[CH:12][C:11]=3[CH3:18])[CH:5]=2)[CH:24]=[CH:23][C:22]=1[O:25][CH3:26]

参加物

5

実験手順

To a suspension of 2-chloro-3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-4-(2,4,6-trimethylphenylimino)pyrimidine (1.0 g) in a mixture of methanol (9 ml) and water (1.5 ml) was added sodium azide (0.163 g). The mixture was stirred at 50° to 55° C. for an hour. After removal of the solvent, the residue was washed with water and collected by filtration to give 4,5-dihydro-7-(3,4-dimethoxyphenyl)-4-methyl-5-(2,4,6-trimethylphenylimino)tetrazolo[1,5-a]pyrimidine (0.80 g).

後処理

  1. customAfter removal of the solvent
  2. washthe residue was washed with water
  3. filtrationcollected by filtration

出典と根拠

ORDレコード
ord-40ed55c10e9f410d8fb8ab45b4b32b5c
出典データセット
uspto-grants-1988_02
特許番号
US04725600

関連ノート

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