1-(3-nitrophenyl)-1H-tetrazol-5-ol → 1-(3-aminophenyl)-1,4-dihydro-5H-tetrazol-5-one

HRID 59047ノート

反応式

HRID 59047 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]([N:10]2[C:14](=[O:15])[NH:13][N:12]=[N:11]2)[CH:7]=[CH:8][CH:9]=1)([O-])=O>[Pd].CO>[NH2:1][C:4]1[CH:5]=[C:6]([N:10]2[C:14](=[O:15])[NH:13][N:12]=[N:11]2)[CH:7]=[CH:8][CH:9]=1

参加物

4

反応物 1

HCID 1360089101-(3-nitrophenyl)-1H-tetrazol-5-ol

生成物 1

HCID 1360622141-(3-aminophenyl)-1,4-dihydro-5H-tetrazol-5-one

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A mixture of 1-(3-nitrophenyl)-1,4-dihydro-5H-tetrazol-5-one (130 mg, 0.63 mmol) and palladium on charcoal (Aldrich Cat. No. 330108; 13 mg) in MeOH (10 mL) was hydrogenated at 20 psi for 3 hr. The mixture was then filtered through celite and the filter cake washed with MeOH (×3). The filtrate was concentrated under vacuum to leave the product, which was used directly in the next step (yield assumed quantitative=111 mg).

後処理

  1. filtrationThe mixture was then filtered through celite
  2. washthe filter cake washed with MeOH (×3)
  3. concentrationThe filtrate was concentrated under vacuum
  4. customto leave the product, which
  5. customwas used directly in the next step (yield assumed quantitative=111 mg)

出典と根拠

ORDレコード
ord-2816d3e285c14bcba54cbb4376f7f490
出典データセット
uspto-grants-2016_09
特許番号
US09439888B2

反応ノート

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