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Triethylamine → 4-(Pyridin-3-ylsulfamoylmethyl)benzoic Acid Methyl Ester

HRID 1727261
ノート
印刷プレビュー

反応式

HRID 1727261 の反応式
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][S:11](Cl)(=[O:13])=[O:12])=[CH:6][CH:5]=1.[NH2:16][C:17]1[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=1.C(N(CC)CC)C>C(Cl)Cl.C(Cl)(Cl)Cl>[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][S:11](=[O:13])(=[O:12])[NH:16][C:17]2[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=2)=[CH:6][CH:5]=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 3

HCID 8471TriethylamineHCID 100093-AminopyridineHCID 21804301Methyl 4-[(chlorosulfonyl)methyl]benzoate

生成物 1

HCID 303913014-(Pyridin-3-ylsulfamoylmethyl)benzoic Acid Methyl Ester収率 81%

試薬・触媒・溶媒 2

HCID 6212Chloroform溶媒HCID 6344Dichloromethane
溶媒

実験手順

To a solution of 4-chlorosulfonylmethylbenzoic acid methyl ester (435 mg, 1.75 mmol) and 3-aminopyridine (170 mg, 1.81 mmol) in CH2Cl2 (10 mL) at 0° C. was added triethylamine (488 μL, 3.50 mmol), and the mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with CHCl3, and the mixture was washed with water and brine. The organic layer was dried (Na2SO4) and evaporated under reduced pressure to give the crude product which was purified by MPLC on silica gel (3% MeOH in EtOAc) to afford the titled compound (434 mg, 81%) as a white solid.

後処理

  1. washthe mixture was washed with water and brine
  2. dry with materialThe organic layer was dried (Na2SO4)
  3. customevaporated under reduced pressure
  4. customto give the crude product which
  5. customwas purified by MPLC on silica gel (3% MeOH in EtOAc)

出典と根拠

ORDレコード
ord-4375fbc633ca40edbdfe4b1fa0651bbc
出典データセット
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07495022B2

反応ノート

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