benzyl 6-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-ylcarbamate → 6-(4-Cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amine

HRID 1040227Notes

Reaction equation

HRID 1040227 reaction equation
[CH:1]1([N:4]2[CH:8]=[N:7][N:6]=[C:5]2[C:9]2[N:14]=[C:13]([NH:15]C(=O)OCC3C=CC=CC=3)[CH:12]=[CH:11][CH:10]=2)[CH2:3][CH2:2]1>[Pd]>[CH:1]1([N:4]2[CH:8]=[N:7][N:6]=[C:5]2[C:9]2[N:14]=[C:13]([NH2:15])[CH:12]=[CH:11][CH:10]=2)[CH2:3][CH2:2]1

Participants

3

Reactant 1

HCID 66851549benzyl 6-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-ylcarbamate

Product 1

HCID 581029666-(4-Cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amineYield 100.2%

Reagents, catalysts & solvents 1

HCID 23938PalladiumCatalyst

Procedure

A mixture of benzyl 6-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-ylcarbamate (660 mg, 1.96 mmol, 1.0 eq) and Pd/C (80 mg 10% Pd loading, 40 mg/mmol) was loaded into a flask and purged with nitrogen. Ethanol (0.4 M) was added and the flask was charged with hydrogen (1 atm balloon pressure). The reaction was stirred at room temperature for 90 minutes, and judged to be complete by TLC. The reaction mixture was filtered through celite, and concentrated under reduced pressure to give 395 mg (95%) of 6-(4-cyclopropyl-4H-[1,2,4]triazol-3-yl)-pyridin-2-ylamine. C10H11N5. 202.1 (M+1). 1H NMR (DMSO) d 8.14 (s, 1H), 7.54 (t, J=8 Hz, 1H), 7.46 (d, J=7 Hz, 1H), 6.60 (d, J=8 Hz, 1H), 4.70 (br s, 2H), 3.85-3.88 (m, 1H), 1.04-1.07 (m, 2H), 0.85-0.88 (m, 2H).

Workup

  1. customwas loaded into a flask
  2. custompurged with nitrogen
  3. additionEthanol (0.4 M) was added
  4. additionthe flask was charged with hydrogen (1 atm balloon pressure)
  5. filtrationThe reaction mixture was filtered through celite
  6. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-5c7fc459bb754138b85d04f43c5bc389
Source dataset
uspto-grants-2013_10
Patent number
US08552196B2

Reaction notes

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