Methanol → 2'-Methyl-2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinolin]-7'-amine

HRID 2088760ノート

反応式

HRID 2088760 の反応式
Cl.Cl.[CH3:3][N:4]1[CH2:13][C:12]2([CH2:15][CH2:14]2)[C:11]2[C:6](=[CH:7][C:8]([NH2:16])=[CH:9][CH:10]=2)[CH2:5]1.[OH-].[Na+].CO>C(Cl)(Cl)Cl>[CH3:3][N:4]1[CH2:13][C:12]2([CH2:15][CH2:14]2)[C:11]2[C:6](=[CH:7][C:8]([NH2:16])=[CH:9][CH:10]=2)[CH2:5]1

参加物

5

反応物 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 670752002'-methyl-2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinolin]-7'-amine dihydrochloride

生成物 1

HCID 445958982'-Methyl-2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinolin]-7'-amine収率 102.3%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

To a stirred suspension of 2′-methyl-2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-isoquinolin]-7′-amine dihydrochloride (1.90 kg, 7.27 mol, 1.09 eq.) in chloroform (19 L) at room temperature was added 5 N NaOH (3.8 L), and the mixture was stirred for 5 minutes. The chloroform layer was separated and the aqueous layer was extracted with chloroform (9.5 L). Combined chloroform layers were washed with 5% aqueous NaCl (9.5 L), then dried over anhydrous sodium sulfate (3.8 kg) for 1 hour. Sodium sulfate was filtered and washed with chloroform (3.8 L). Combined filtrate and washing were evaporated to give crude oil. Methanol (4.6 L) was added and the solution was evaporated to give 2′-methyl-2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-isoquinolin]-7′-amine (1.40 kg) as brownish crystals in crude 102% recovery.

後処理

  1. customThe chloroform layer was separated
  2. extractionthe aqueous layer was extracted with chloroform (9.5 L)
  3. washCombined chloroform layers were washed with 5% aqueous NaCl (9.5 L)
  4. dry with materialdried over anhydrous sodium sulfate (3.8 kg) for 1 hour
  5. filtrationSodium sulfate was filtered
  6. washwashed with chloroform (3.8 L)
  7. washCombined filtrate and washing
  8. customwere evaporated
  9. customto give crude oil
  10. customthe solution was evaporated

出典と根拠

ORDレコード
ord-c45ffa459f6d47f89c20c01eceee5425
出典データセット
uspto-grants-2013_05
特許番号
US08436004B2

反応ノート

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