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Toluene → HCID 178469938、化合物

HRID 1161504
ノート
印刷プレビュー

反応式

HRID 1161504 の反応式
FC(F)(F)C(O)=O.[CH2:8]([O:10][C:11]([C:13]1[C:14]([NH:18][NH:19]C(OC(C)(C)C)=O)=[N:15][NH:16][CH:17]=1)=[O:12])[CH3:9].C1(C)C=CC=CC=1.[Cl:34]CCl>>[ClH:34].[ClH:34].[CH2:8]([O:10][C:11]([C:13]1[C:14]([NH:18][NH2:19])=[N:15][NH:16][CH:17]=1)=[O:12])[CH3:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 1140TolueneHCID 6344DichloromethaneHCID 6422Trifluoroacetic acidHCID 178469939HCID 178469939、化合物

生成物 1

HCID 178469938HCID 178469938、化合物

実験手順

After adding 25 ml of trifluoroacetic acid to a solution of 3.30 g of 3-(N′-t-butoxycarbonylhydrazino)-1H-pyrazole-4-carboxylic acid ethyl ester in 50 ml of dichloromethane, the mixture was stirred for 2 hours at room temperature. Next, 100 ml of toluene was added and the solvent was removed under reduced pressure. The residue was dissolved in a small amount of methanol, and after adding a 4N solution containing hydrochloric acid in ethyl acetate until the solution reached acidic, the solvent was removed under reduced pressure. The residue was treated with 50 ml of t-butyl methyl ether, and the solid was filtered off and dried under reduced pressure to give the title compound (3.30 g) as a white solid.

後処理

  1. customthe solvent was removed under reduced pressure
  2. dissolutionThe residue was dissolved in a small amount of methanol
  3. additionafter adding a 4N solution
  4. additioncontaining hydrochloric acid in ethyl acetate until the solution
  5. customthe solvent was removed under reduced pressure
  6. additionThe residue was treated with 50 ml of t-butyl methyl ether
  7. filtrationthe solid was filtered off
  8. customdried under reduced pressure

出典と根拠

ORDレコード
ord-34fb8ef4ab7d4f598a9f62230e6b8984
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07816522B2

反応ノート

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