Tetrahydrofuran → 3-Amino-pyridine-2-sulfonic acid quinolin-8-ylamide

HRID 513589

反応式

HRID 513589 の反応式
[NH4+].[Cl-].[N:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[NH:13][S:14]([C:17]2[C:22]([N+:23]([O-])=O)=[CH:21][CH:20]=[CH:19][N:18]=2)(=[O:16])=[O:15])[CH:6]=[CH:5][CH:4]=1.C1COCC1>CO.[Zn]>[N:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[NH:13][S:14]([C:17]2[C:22]([NH2:23])=[CH:21][CH:20]=[CH:19][N:18]=2)(=[O:16])=[O:15])[CH:6]=[CH:5][CH:4]=1

参加物

6

反応物 3

HCID 8028TetrahydrofuranHCID 25517Ammonium ChlorideHCID 681832803-Nitro-pyridine-2-sulfonic acid quinolin-8-ylamide2 回

生成物 1

HCID 681831363-Amino-pyridine-2-sulfonic acid quinolin-8-ylamide収率 95.1%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 887Methanol溶媒

実験手順

Sat. NH4Cl (0.49 g, 9.09 mmol) was added to a solution of 3-nitro-pyridine-2-sulfonic acid quinolin-8-ylamide (Intermediate 259) (0.3 g, 0.91 mmol) in MeOH:THF(10 ml, 1:1) followed by zinc powder (0.48 g, 7.27 mmol) and the mixture was stirred at room temperature for 18 h. The mixture was filtered through celite and washed with THF. The filtrate was concentrated in vacuo and the residue was diluted with EtOAc. The organic phase was dried (Na2SO4) and concentrated in vacuo. The crude residue was purified by column chromatography with DCM/MeOH as the eluent to give the title compound (0.26 g, 95%)

後処理

  1. filtrationThe mixture was filtered through celite
  2. washwashed with THF
  3. concentrationThe filtrate was concentrated in vacuo
  4. additionthe residue was diluted with EtOAc
  5. dry with materialThe organic phase was dried (Na2SO4)
  6. concentrationconcentrated in vacuo
  7. customThe crude residue was purified by column chromatography with DCM/MeOH as the eluent

出典と根拠

ORDレコード
ord-59ab7fdbcc13496aae95b9865214ee63
出典データセット
uspto-grants-2015_08
特許番号
US09102688B2

関連ノート

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