Tetrahydrothiopyran-4-one → 10-amino-3,4-dihydro-7-trifluoromethyl-1H-thiopyrano[4,3-b]quinoline

HRID 1195714ノート

反応式

HRID 1195714 の反応式
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:4]=[C:5]([NH2:11])[C:6](=[CH:9][CH:10]=1)[C:7]#[N:8].[S:14]1[CH2:19][CH2:18][C:17](=O)[CH2:16][CH2:15]1>[N+](C1C=CC=CC=1)([O-])=O.[Cl-].[Zn+2].[Cl-]>[NH2:8][C:7]1[C:6]2[CH:9]=[CH:10][C:3]([C:2]([F:12])([F:13])[F:1])=[CH:4][C:5]=2[N:11]=[C:17]2[CH2:18][CH2:19][S:14][CH2:15][C:16]=12

参加物

5

反応条件

温度
50 °C

実験手順

To a solution of 4-trifluoromethyl anthranilonitrile (12.2 g) in 50 ml of nitrobenzene was added freshly fused and pulverized zinc chloride (13.4 g). This was stirred at 50° C. for 1.5 hours after which was added tetrahydrothiopyran-4-one (9.9 g). The reaction mixture was stirred at 130° C. for 2 hours and allowed to cool, and the resulting complex was filtered and rinsed with ethyl ether. The solid was partitioned between 2-butanone (MEK) and NH4OH and the aqueous phase was extracted with MEK (2x). The organics were washed with water, dried (saturated NaCl, MgSO4) and concentrated to give 10.2 g of a yellow powder m.p. 253°-259° C.d. A 3.7 g portion was recrystallized from methanol/water to give 3.0 g of an off-white powder, m.p. 258°-262° C. d.

後処理

  1. stirringThe reaction mixture was stirred at 130° C. for 2 hours
  2. temperatureto cool
  3. filtrationthe resulting complex was filtered
  4. washrinsed with ethyl ether
  5. customThe solid was partitioned between 2-butanone (MEK) and NH4OH
  6. extractionthe aqueous phase was extracted with MEK (2x)
  7. washThe organics were washed with water
  8. dry with materialdried (saturated NaCl, MgSO4)
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-9d60d9b8daa6406d8165a3c64dbfa6df
出典データセット
uspto-grants-1992_05
特許番号
US05112830

反応ノート

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