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Ammonium Chloride → N-(5-amino-4-chloro-2-methylphenyl)methanesulfonamide

HRID 889447
ノート
印刷プレビュー

反応式

HRID 889447 の反応式
[Cl:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([NH:11][S:12]([CH3:15])(=[O:14])=[O:13])=[C:4]([CH3:16])[CH:3]=1.[Cl-].[NH4+]>C(O)C.O.[Zn]>[NH2:8][C:7]1[C:2]([Cl:1])=[CH:3][C:4]([CH3:16])=[C:5]([NH:11][S:12]([CH3:15])(=[O:14])=[O:13])[CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 25517Ammonium ChlorideHCID 67359857N-(4-chloro-2-methyl-5-nitrophenyl)methanesulfonamide

生成物 1

HCID 67357473N-(5-amino-4-chloro-2-methylphenyl)methanesulfonamide収率 96.2%

試薬・触媒・溶媒 3

HCID 23994Zinc触媒HCID 702Ethanol溶媒HCID 962Water
溶媒

実験手順

A mixture of Intermediate 79A (175 mg, 0.66 mmol), zinc (432 mg, 6.61 mmol), ammonium chloride (354 mg, 6.61 mmol) in ethanol (10 mL) and water (5.0 mL) was heated to reflux for 30 min. The reaction mixture was concentrated, suspended in ethyl acetate and filtered. The filtrate was washed with water, aqueous NaHCO3 and brine, dried over MgSO4 and concentrated to give Intermediate 79 (149 mg, 96%) as a white solid. HPLC: Rt=0.453 min. (CHROMOLITH® column 4.6×50 mm eluting with 10-90% aqueous methanol over 4 min. containing 0.1% TFA, 4 mL/min., monitoring at 220 nm). MS (ES): m/z=235 [M+H]+. Intermediate 79 was used in the synthesis of Example 243.

後処理

  1. temperaturewas heated
  2. temperatureto reflux for 30 min
  3. concentrationThe reaction mixture was concentrated
  4. filtrationfiltered
  5. washThe filtrate was washed with water, aqueous NaHCO3 and brine
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-fce048a090fd4352840d139c20efe8fb
出典データセット
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08252795B2

反応ノート

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