HCID 15490830, compound → HCID 22243668, compound

HRID 2220743Notes

Reaction equation

HRID 2220743 reaction equation
[C:1]([O:5][C:6]([NH:8][CH:9]([CH2:13][NH:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[N+:21]([O-])=O)[C:10]([OH:12])=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2]>CCO.[Pd]>[NH2:21][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[NH:14][CH2:13][CH:9]([NH:8][C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[C:10]([OH:12])=[O:11]

Participants

4

Procedure

A suspension of 1.0 eq of 89 and 0.1 wt/wt eq of 10% Pd on carbon in 35 mL of EtOH was hydrogenated under 50 psi of H2 for 30 min, until consumption of H2 ceased. The reaction mixture was filtered through Celite. The filtrate was concentrated by rotary evaporation. The crude material was dried under vacuum to give acid 90.

Workup

  1. customwas hydrogenated under 50 psi of H2 for 30 min, until consumption of H2
  2. filtrationThe reaction mixture was filtered through Celite
  3. concentrationThe filtrate was concentrated by rotary evaporation
  4. dry with materialThe crude material was dried under vacuum

Sources & evidence

ORD record
ord-25f75a61967b4bbfb4d5439bc5f996c6
Source dataset
uspto-grants-2008_08
Patent number
US07417152B2

Reaction notes

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