1,1-Dichloroethane → 3-[[N-(5,5-dimethyl-1-pyrrolin-2-yl)-p-anisidino]methyl]indole hydrochloride

HRID 1758349ノート

反応式

HRID 1758349 の反応式
P(Cl)(Cl)([Cl:3])=O.[CH3:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([NH:14][CH2:15][C:16]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[NH:18][CH:17]=2)=[CH:10][CH:9]=1.[CH3:25][C:26]1([CH3:32])[NH:30][C:29](=O)[CH2:28][CH2:27]1.C(N(CC)CC)C.ClC(Cl)C.[OH-].[Na+]>ClCCCl>[ClH:3].[CH3:25][C:26]1([CH3:32])[N:30]=[C:29]([N:14]([CH2:15][C:16]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[NH:18][CH:17]=2)[C:11]2[CH:12]=[CH:13][C:8]([O:7][CH3:6])=[CH:9][CH:10]=2)[CH2:28][CH2:27]1

参加物

8

反応物 6

HCID 63651,1-DichloroethaneHCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 918780N-((1H-indol-3-yl)methyl)-4-methoxyanilineHCID 111262105,5-dimethylpyrrolidin-2-one

生成物 1

HCID 205097773-[[N-(5,5-dimethyl-1-pyrrolin-2-yl)-p-anisidino]methyl]indole hydrochloride収率 19.8%

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

Phosphorus oxychloride (1.53 g., 0.01 mole), 3-(p-anisidinomethyl)indole, (2.52 g., 0.01 mole), 5,5-dimethyl-2-pyrrolidinone (1.13 g., 0.01 mole), and triethylamine (1.01 g., 0.01 mole) in 50 ml. of 1,2-dichloroethane is reacted according to the procedure of Example 36. After standing for 6 hr. at ice bath temperature, the reaction mixture is filtered affording the crude hydrochloride salt (1.45 g.) of the product, m.p. 188°-191° C. The dichloroethane filtrate is made basic with 10% sodium hydroxide, separated, dried over magnesium sulfate, acidified with ethanolic hydrogen chloride, and concentrated under reduced pressure. Trituration of the residue thus obtained with aceton yields a second crop of the hydrochloride, (0.76 g.), m.p. 191°-194° C. The hydrochloride fractions are combined and converted to the free base (m.p. 83°-85° C.) in the usual manner by dissolving in water and making basic with sodium hydroxide followed by extraction with ether. The hydrochloride salt is reprepared by taking the free base up in ethanol and acidifying with ethanolic hydrogen chloride to provide analytically pure 3-[[N-(5,5-dimethyl-1-pyrrolin-2-yl)-p-anisidino]methyl]indole hydrochloride, m.p. 188.5°-190.5° C. (dec.) (corr.)

後処理

  1. filtrationat ice bath temperature, the reaction mixture is filtered
  2. customaffording the crude hydrochloride salt (1.45 g.) of the product, m.p. 188°-191° C
  3. customseparated
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customTrituration of the residue thus obtained with aceton

出典と根拠

ORDレコード
ord-32b4cbd782db42498cbc6af6c8a8a8db
出典データセット
uspto-grants-1983_02
特許番号
US04372887

反応ノート

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