Phosphorus oxychloride → HCID 13787234, compound

HRID 1194537Notes

Reaction equation

HRID 1194537 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]([C:11]2[CH:12]=[N:13][C:14]3[CH2:15][CH2:16][CH2:17][CH2:18][C:19]=3[C:20]=2O)=[O:10])=[CH:4][CH:3]=1.P(Cl)(Cl)([Cl:24])=O>>[Cl:24][C:20]1[C:19]2[CH2:18][CH2:17][CH2:16][CH2:15][C:14]=2[N:13]=[CH:12][C:11]=1[C:9](=[O:10])[NH:8][C:5]1[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=1

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 178522065HCID 178522065, compound

Product 1

HCID 13787234HCID 13787234, compound

Procedure

A mixture of 1.0 g of 3-(N-p-chlorophenylcarbamoyl)4-hydroxy-5,6,7,8-tetrahydroquinoline (Example 17a) and 25 mL of phosphorous oxychloride is heated at 80° for 3 hours to obtain a clear solution, and evaporated to dryness. The residue is treated with 400 mL of a 1:1 mixture of ice cold 2N aqueous sodium hydroxide and dichloromethane. The organic phase is separated, dried and evaporated to yield the 4-chloro-3-(N-p-chlorophenylcarbamoyl)-5,6,7,8-tetrahydroquinoline. The mixture of 0.6 g thereof, 1.0 g of O-methylhydroxylamine hydrochloride and 1.65 g of diisopropylethylamine is heated to 100° in a small pressure vessel for 18 hours. The cooled mixture is then triturated with water, dissolved in tetrahydrofuran, dried and evaporated to yield the 4-(O-methylhydroxylamino)-3-(N-p- chlorophenylcarbamoyl)-5,6,7,8-tetrahydroquinoline.

Workup

  1. temperatureis heated at 80° for 3 hours
  2. customto obtain a clear solution
  3. customevaporated to dryness
  4. additionThe residue is treated with 400 mL of a 1:1 mixture of ice cold 2N aqueous sodium hydroxide and dichloromethane
  5. customThe organic phase is separated
  6. customdried
  7. customevaporated

Sources & evidence

ORD record
ord-d065e41fdb854547b76aad190ca4bfaa
Source dataset
uspto-grants-1989_03
Patent number
US04814450

Reaction notes

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