HCID 21450339, compound → HCID 21450328, compound

HRID 596589Notes

Reaction equation

HRID 596589 reaction equation
[CH3:1][CH:2]([C:5]1[N:10]=[C:9]([N+:11]([O-])=O)[C:8]([OH:14])=[CH:7][CH:6]=1)[CH2:3][CH3:4]>[Pd].CO>[NH2:11][C:9]1[C:8]([OH:14])=[CH:7][CH:6]=[C:5]([CH:2]([CH3:1])[CH2:3][CH3:4])[N:10]=1

Participants

4

Procedure

6-(1-methylpropyl)-3-hydroxy-2-nitropyridine (23 g.) in 450 ml. of methanol is hydrogenated over 1 gm. of 5% palladium on carbon catalyst for 3 hours. The catalyst is removed on a filter and the filtrate is concentrated to dryness to give 2-amino-3-hydroxy-6-(1-methylpropyl)pyridine.

Workup

  1. customThe catalyst is removed on
  2. filtrationa filter
  3. concentrationthe filtrate is concentrated to dryness

Sources & evidence

ORD record
ord-34e1a4d30b794b70b3f954b91d990fde
Source dataset
uspto-grants-1977_03
Patent number
US04011326

Reaction notes

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