HCID 19761221, compound → HCID 19761240, compound

HRID 249341Notes

Reaction equation

HRID 249341 reaction equation
C([N:8]1[CH2:13][CH2:12][CH:11]([N:14]([CH3:20])[C:15](=[O:19])[O:16][CH2:17][CH3:18])[CH2:10][CH2:9]1)C1C=CC=CC=1>C(O)(=O)C.[Pd]>[NH:8]1[CH2:9][CH2:10][CH:11]([N:14]([CH3:20])[C:15](=[O:19])[O:16][CH2:17][CH3:18])[CH2:12][CH2:13]1

Participants

4

Procedure

49 g of the compound obtained in Stage A dissolved in 500 ml of acetic acid in the presence of 1 g of 5% Pd/C are hydrogenated at 50° C. under 5 Kg. The catalyst is filtered off, the filtrate is evaporated, recovered with diethyl ether and rendered basic in the cold with 50 ml of sodium hydroxide solution. The ethereal phase is dried and evaporated to yield the desired compound.

Workup

  1. customare hydrogenated at 50° C. under 5 Kg
  2. filtrationThe catalyst is filtered off
  3. customthe filtrate is evaporated
  4. customrecovered with diethyl ether
  5. customThe ethereal phase is dried
  6. customevaporated

Sources & evidence

ORD record
ord-17f2de49c2554de2bbe0f48ac0105a6e
Source dataset
uspto-grants-1993_05
Patent number
US05214055

Reaction notes

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