HCID 22719847, compound → HCID 22719889, compound

HRID 1582174Notes

Reaction equation

HRID 1582174 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([OH:16])[CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=2)=[CH:4][CH:3]=1>C(O)(=O)C.[OH-].[Na+].[Pt]=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([OH:16])[CH2:9][CH:10]2[CH2:15][CH2:14][CH2:13][CH2:12][NH:11]2)=[CH:4][CH:3]=1

Participants

5

Procedure

1 mmol of the compound obtained in Example 58 is dissolved in 20 ml of acetic acid, and 8 mg of platinum oxide are added. The hydrogenation is carried out starting from an initial pressure of 3 atmospheres at 24° C. After reacting for 3 hours, the catalyst is filtered off and washed with dichloromethane. The solvents are evaporated off and the residue obtained is dissolved in 10% sodium hydroxide solution and extracted with dichloromethane. The organic phase is washed with water, dried over MgSO4 and then evaporated off to yield the title compound in the form of a white solid.

Workup

  1. customat 24° C
  2. filtrationthe catalyst is filtered off
  3. washwashed with dichloromethane
  4. customThe solvents are evaporated off
  5. customthe residue obtained
  6. extractionextracted with dichloromethane
  7. washThe organic phase is washed with water
  8. dry with materialdried over MgSO4
  9. customevaporated off

Sources & evidence

ORD record
ord-b3c42a3be9324cebb453afcb897690aa
Source dataset
uspto-grants-2004_05
Patent number
US06734196B2

Reaction notes

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