Isobutyryl chloride → HCID 67499511, compound

HRID 1428334Notes

Reaction equation

HRID 1428334 reaction equation
[C:1](Cl)(=[O:5])[CH:2]([CH3:4])[CH3:3].[CH3:7][NH:8][C:9]1[CH:10]=[N:11][N:12]([C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)[CH:13]=1>ClC(Cl)C>[CH3:7][N:8]([C:9]1[CH:10]=[N:11][N:12]([C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)[CH:13]=1)[C:1](=[O:5])[CH:2]([CH3:4])[CH3:3]

Participants

4

Reactant 2

HCID 62325Isobutyryl chlorideHCID 67499383HCID 67499383, compound

Product 1

HCID 67499511HCID 67499511, compoundYield 54.3%

Reagents, catalysts & solvents 1

HCID 63651,1-DichloroethaneSolvent3×

Procedure

A solution of isobutyryl chloride (0.138 g, 1.3 mmol) in dichloroethane (1 mL) was pipetted at a dropwise rate into an ice-cold suspension of methyl-(1-pyridin-3-yl-1H-pyrazol-4-yl)-amine (0.15 g, 0.86 mmol) in dichloroethane (5 mL), stirred for 10 minutes and then treated at a dropwise rate with a solution of 4-N,N-dimethylaminopyridine (0.11 g, 0.9 mmol) in dichloroethane (1.5 mL). The cooling bath was removed after 30 minutes, stirred under nitrogen at room temperature for 14 hours, diluted with dichloroethane (40 mL), washed with water (30 mL), brine (10 mL), dried over MgSO4 and purified by reversed phase column chromatography to give a yellowish gum (0.114 g, 54%) 1H NMR (300 MHz, CDCl3) δ 9.01-8.93 (m, 1H), 8.67 (s, 0.4H), 8.61 (d, J=4.2 Hz, 0.6H), 8.54 (d, 0.4H), 8.08-8.02 (m, 1H), 7.96 (s, 0.6H), 7.80 (s, 0.4H), 7.70 (s, 0.6H), 7.47-7.37 (m, 1H), 3.49 (s, 1.2H), 3.26 (s, 2.8H), 3.06-2.98 (m, 0.4H), 2.86-2.70 (m, 0.6H), 1.25 (d, J=6.1 Hz, 2.4H), 1.09 (d, J=6.6 Hz, 3.6H). ESIMS m/z 245 ([M+1]).

Workup

  1. customThe cooling bath was removed after 30 minutes
  2. stirringstirred under nitrogen at room temperature for 14 hours
  3. additiondiluted with dichloroethane (40 mL)
  4. washwashed with water (30 mL), brine (10 mL)
  5. dry with materialdried over MgSO4
  6. custompurified by reversed phase column chromatography

Sources & evidence

ORD record
ord-79e30f76115c4b9397580f8c154aef6c
Source dataset
uspto-grants-2015_01
Patent number
US08937083B2

Reaction notes

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