HCID 118022928, compound → 3-(3-chloro-1H-pyrazol-1-yl)pyridine

HRID 1482408Notes

Reaction equation

HRID 1482408 reaction equation
[Cl:1][C:2]1[CH2:6][CH2:5][N:4]([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=2)[N:3]=1>ClC1C=CC=CC=1.[O-2].[Mn+4].[O-2]>[Cl:1][C:2]1[CH:6]=[CH:5][N:4]([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=2)[N:3]=1

Participants

4

Conditions

Temperature
80 °C

Procedure

A mixture of 3-chloro-4,5-dihydro-1-(3-pyridinyl)-1H-pyrazole (0.182 g, 1.00 mmol) and manganese (IV) oxide (0.870 g, 10.0 mmol) (Carus black) in chlorobenzene (2 mL) was heated at 80° C. for 24 hours. The mixture was allowed to cool to room temperature, filtered through Celite®, and the wetcake was rinsed with chlorobenzene (2 mL). The lightly tinted solution was acidified with hydrochloric acid (4 M in 1,4-dioxane) to ˜pH 1.5 to give a thick, white mixture. After stirring in an ice-bath for 30 minutes, the mixture was filtered through a sintered glass funnel and rinsed with cold chlorobenzene (2 mL). The solids (0.380 g) were allowed to air-dry in a hood overnight to give the title compound as an off-white solid (0.140 g, 64%, LC internal standard analysis indicated a purity of 98.7 wt %): mp 229-237° C.; 1H NMR (DMSO-d6) δ 11.11 (bs, 1H), 9.27 (d, J=2.4 Hz, 1H), 8.82 (d, J=2.7 Hz, 1H), 8.71 (dd, J=5.1, 1.2 Hz, 1H), 8.61 (ddd, J=8.5, 2.5, 1.2 Hz, 1H), 7.89 (dd, J=8.5, 5.1 Hz, 1H), 6.79 (d, J=2.7 Hz, 1H).

Workup

  1. temperatureto cool to room temperature
  2. filtrationfiltered through Celite®
  3. washthe wetcake was rinsed with chlorobenzene (2 mL)
  4. customto give a thick, white mixture
  5. filtrationthe mixture was filtered through a sintered glass funnel
  6. washrinsed with cold chlorobenzene (2 mL)
  7. customto air-dry in a hood overnight

Sources & evidence

ORD record
ord-c93b6db43c354694919c5d644665205f
Source dataset
uspto-grants-2016_08
Patent number
US09414594B2

Reaction notes

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