Stannous Chloride → 3-hydrazino-N-methoxy-4-methyl-benzamide

HRID 251329

反応式

HRID 251329 の反応式
[NH2:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[CH3:13])[C:5]([NH:7][O:8][CH3:9])=[O:6].[N:14]([O-])=O.[Na+].[Sn](Cl)Cl>O.Cl>[NH:1]([C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[CH3:13])[C:5]([NH:7][O:8][CH3:9])=[O:6])[NH2:14]

参加物

6

反応物 3

HCID 24479Stannous ChlorideHCID 207670003-Amino-N-methoxy-4-methylbenzamideHCID 23668193Sodium Nitrite

生成物 1

HCID 116153463-hydrazino-N-methoxy-4-methyl-benzamide

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒2 回HCID 962Water溶媒

反応条件

温度
0 °C

実験手順

To a stirred solution of 3-amino-N-methoxy-4-methyl-benzamide 1 (102 mg, 0.56 mmol, preparation: International Patent Application Publication No. WO 02/40486 A2, pg. 66) in water (5 ml) at 0° C. was added conc. HCl (5 mL) followed by the addition of sodium nitrite (43 mg, 0.62 mmol). The reaction mixture was stirred at 0° C. for 40 min then a solution of tin(II)chloride (241 mg, 1.27 mmol) in conc. HCl (1 mL) was added and the mixture was stirred for 1 hr then allowed to stand at −20° C. for 20 hr before it was warmed to RT and concentrated to a white solid. The solid was triturated with ethanol, the solids were filtered, and the filtrate concentrated to provide 3-hydrazino-N-methoxy-4-methyl-benzamide 2 as white solid (486 mg) as a mixture with tin salts and ethanol which was used without further purification. HPLC (6 minute gradient) tR 0.78 min; MS m/z 195.9 [M+H]+.

後処理

  1. stirringthe mixture was stirred for 1 hr
  2. waitto stand at −20° C. for 20 hr before it
  3. temperaturewas warmed to RT
  4. concentrationconcentrated to a white solid
  5. customThe solid was triturated with ethanol
  6. filtrationthe solids were filtered
  7. concentrationthe filtrate concentrated

出典と根拠

ORDレコード
ord-a7bdf41c70e34209a7b8c11c078333ec
出典データセット
uspto-grants-2011_01
特許番号
US07863314B2

関連ノート

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