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Hydrochloric Acid → HCID 20183601、化合物

HRID 255536
ノート
印刷プレビュー

反応式

HRID 255536 の反応式
[ClH:1].[NH2:2][C:3]1[CH:4]=[N:5][C:6]2[C:11]([C:12]=1[NH:13][CH3:14])=[CH:10][C:9]([CH3:15])=[CH:8][CH:7]=2.[C:16]([OH:20])(=O)[CH2:17][OH:18].Cl.[OH-].[Na+]>>[OH2:18].[ClH:1].[CH3:14][N:13]1[C:12]2[C:11]3[CH:10]=[C:9]([CH3:15])[CH:8]=[CH:7][C:6]=3[N:5]=[CH:4][C:3]=2[N:2]=[C:17]1[CH2:16][OH:20]
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 313Hydrochloric AcidHCID 757Glycolic AcidHCID 14798Sodium HydroxideHCID 13958355HCID 13958355、化合物

生成物 1

HCID 20183601HCID 20183601、化合物

実験手順

A mixture of 4.5 g (0.020 mole) of 3-amino-6-methyl-4-(methylamino)quinoline hydrochloride (from Example 32), 3.8 g (0.050 mole) of glycolic acid and 75 ml of 4 N hydrochloric acid was heated at its reflux temperature for two hours. The solution was cooled, and 50% aqueous sodium hydroxide was then added to make the solution slightly basic. The precipitate was separated by filtration and washed with water. The solid was redissolved in dilute hydrochloric acid and reprecipitated with ammonium hydroxide to provide 1,8-dimethyl-2-hydroxymethyl-1H-imidazo[4,5-c]quinoline hydrochloride hydrate. Analysis: Calculated for C13H13N3O.HCl.H2O: %C, 55.4; %H, 5.7; %N, 14.9; Found: %C, 55.2; %H, 5.6; %N, 15.5.

後処理

  1. temperaturewas heated at its
  2. temperaturereflux temperature for two hours
  3. temperatureThe solution was cooled
  4. customThe precipitate was separated by filtration
  5. washwashed with water
  6. dissolutionThe solid was redissolved in dilute hydrochloric acid
  7. customreprecipitated with ammonium hydroxide

出典と根拠

ORDレコード
ord-46bebac8d1f444df907b4bba0fffa8ca
出典データセット
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04698348

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート