2-Chloro-4-(trifluoromethyl)benzenesulfonyl chloride → N-[3-Acetyl-5-chloro-4-(5-chloro-benzothiazol-2-ylsulfanyl)-phenyl]-2-chloro-4-trifluoromethyl-benzenesulfonamide

HRID 1824399ノート

反応式

HRID 1824399 の反応式
[NH2:1][C:2]1[CH:3]=[C:4]([Cl:22])[C:5]([S:11][C:12]2[S:13][C:14]3[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:15]=3[N:16]=2)=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1.[Cl:23][C:24]1[CH:29]=[C:28]([C:30]([F:33])([F:32])[F:31])[CH:27]=[CH:26][C:25]=1[S:34](Cl)(=[O:36])=[O:35]>N1C=CC=CC=1>[C:8]([C:6]1[CH:7]=[C:2]([NH:1][S:34]([C:25]2[CH:26]=[CH:27][C:28]([C:30]([F:31])([F:32])[F:33])=[CH:29][C:24]=2[Cl:23])(=[O:36])=[O:35])[CH:3]=[C:4]([Cl:22])[C:5]=1[S:11][C:12]1[S:13][C:14]2[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:15]=2[N:16]=1)(=[O:10])[CH3:9]

参加物

4

反応物 2

HCID 27366752-Chloro-4-(trifluoromethyl)benzenesulfonyl chlorideHCID 221489061-[5-Amino-3-chloro2-(5-chloro-benzothiazol-2-ylsulfanyl)-phenyl]-ethanone2 回

生成物 1

HCID 22148793N-[3-Acetyl-5-chloro-4-(5-chloro-benzothiazol-2-ylsulfanyl)-phenyl]-2-chloro-4-trifluoromethyl-benzenesulfonamide収率 72%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
90 °C

実験手順

To a 1M solution of 1-[5-Amino-3-chloro-2-(5-chloro-benzothiazol-2-ylsulfanyl)-phenyl]-ethanone, (265) (4.12 g, 11.19 mmol) in pyridine, obtained from Aldrich, was added 2-chloro-4-trifluoromethyl-benzenesulfonyl chloride (3.75 g, 13.43 mmol) and heated to 90° C. for 1.5 hours. The crude reaction mixture was concentrated under vacuum, partitioned between 2M aqueous HCl (100 mL) and EtOAc (100 mL), and extracted 3 times with EtOAc (100 mL). The combined organic layers were washed twice with saturated aqueous brine (100 mL), dried over Na2SO4, concentrated under vacuum, purified by column chromatography (0–5% Et2O in CH2Cl2), and triturated with CH2Cl2/hexane mixture with 0.5 mL of MeOH added to yield compound 277 (4.9 g, 72%) as an off white solid.

後処理

  1. customThe crude reaction mixture
  2. concentrationwas concentrated under vacuum
  3. custompartitioned between 2M aqueous HCl (100 mL) and EtOAc (100 mL)
  4. extractionextracted 3 times with EtOAc (100 mL)
  5. washThe combined organic layers were washed twice with saturated aqueous brine (100 mL)
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated under vacuum
  8. custompurified by column chromatography (0–5% Et2O in CH2Cl2)
  9. customtriturated with CH2Cl2/hexane mixture with 0.5 mL of MeOH
  10. additionadded

出典と根拠

ORDレコード
ord-17945f3442ba4bfa82a22487b4e4b3e3
出典データセット
uspto-grants-2006_05
特許番号
US07041691B1

反応ノート

読み込み中…