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N-(2-Aminoethyl)isoquinoline-5-sulfonamide → N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamide

HRID 5740
ノート
印刷プレビュー

反応式

HRID 5740 の反応式
[NH2:1][CH2:2][CH2:3][NH:4][S:5]([C:8]1[C:9]2[CH:10]=[CH:11][N:12]=[CH:13][C:14]=2[CH:15]=[CH:16][CH:17]=1)(=[O:7])=[O:6].[Cl:18][C:19]1[CH:28]=[CH:27][C:22]([CH:23]=[CH:24][CH:25]=O)=[CH:21][CH:20]=1.[Na].C(OCC)(=O)C>CO>[Cl:18][C:19]1[CH:28]=[CH:27][C:22]([CH:23]=[CH:24][CH2:25][NH:1][CH2:2][CH2:3][NH:4][S:5]([C:8]2[C:9]3[CH:10]=[CH:11][N:12]=[CH:13][C:14]=3[CH:15]=[CH:16][CH:17]=2)(=[O:7])=[O:6])=[CH:21][CH:20]=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 4

HCID 3544N-(2-Aminoethyl)isoquinoline-5-sulfonamideHCID 8857Ethyl AcetateHCID 3794977p-ChlorocinnamaldehydeHCID 5360545Sodium

生成物 1

HCID 176156N-[2-(4-Chlorocinnamylamino)ethyl]-5-isoquinolinesulfonamide収率 71.5%

試薬・触媒・溶媒 1

HCID 887Methanol
溶媒

実験手順

2.01 g of N-(2-aminoethyl]-5-isoquinolinesulfonamide was dissolved in 30 ml of methanol, to the solution was added 1.60 g of p-chlorocinnamaldehyde, and the mixture was stirred for one hour at a room temperature. After an addition of 350 mg of sodium tetrahydrideborate in portions with ice cooling, the mixture was stirred for 30 minutes. After an addition of ethyl acetate, the reaction mixture was sequentially washed three times with water, and then twice with a saturated sodium chloride aqueous solution, and dried over magnesium sulfate. The mixture was filtered and evaporated to remove the solvent under a reduced pressure. A residue was purified using a silica gel column (silica gel 80 g, eluant: 5% methanol in chloroform), and resulting crystals were washed with benzene/hexane (1:1), to obtain 2.30 g of the title compound as colorless crystals.

後処理

  1. stirringthe mixture was stirred for 30 minutes
  2. washthe reaction mixture was sequentially washed three times with water
  3. dry with materialtwice with a saturated sodium chloride aqueous solution, and dried over magnesium sulfate
  4. filtrationThe mixture was filtered
  5. customevaporated
  6. customto remove the solvent under a reduced pressure
  7. customA residue was purified
  8. customresulting crystals
  9. washwere washed with benzene/hexane (1:1)

出典と根拠

ORDレコード
ord-972b7e9615b641608f2fd7c85b62dfc9
出典データセット
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05245034

反応ノート

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