Quinoline → HCID 70362477, compound

HRID 1638761Notes

Reaction equation

HRID 1638761 reaction equation
[C:1]1([C:7]#[C:8][CH2:9][N:10]2[C:18](=[O:19])[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]2=[O:20])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.N1C2C(=CC=CC=2)C=CC=1>[Pd].CC([O-])=O.CC([O-])=O.[Pb+2].C1COCC1>[C:1]1([CH2:7]/[CH:8]=[CH:9]\[N:10]2[C:18](=[O:19])[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]2=[O:20])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

5

Reactant 2

HCID 7047QuinolineHCID 808056AG-777/36181001

Product 1

HCID 70362477HCID 70362477, compound

Reagents, catalysts & solvents 2

HCID 131709914Lindlars catalystCatalystHCID 8028TetrahydrofuranSolvent

Procedure

The title compound was prepared from the title product (15 g, 57.4 mmol) of Example 153 by hydrogenation using Lindlar catalyst (2.25 g) and quinoline (0.79 g, 6.09 mmol) in THF (150 ml). The reaction mixture was hydrogenated at 5 psi and 0° to obtain a quantitative yield of the cis product.

Workup

  1. customwas hydrogenated at 5 psi and 0°
  2. customto obtain a quantitative yield of the cis product

Sources & evidence

ORD record
ord-cdcbbd34dc6b49d989fc874c6aec430f
Source dataset
uspto-grants-1989_11
Patent number
US04880829

Reaction notes

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