Dichloromethane → HCID 67409996, compound

HRID 570192Notes

Reaction equation

HRID 570192 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH3:16])[N:8]=[C:9]([C:11]([CH3:15])([CH3:14])[CH2:12][F:13])[CH:10]=1)=[O:5])[CH3:2].C(Cl)[Cl:18]>>[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH3:16])[N:8]=[C:9]([C:11]([CH3:15])([CH3:14])[CH2:12][F:13])[C:10]=1[Cl:18])=[O:5])[CH3:2]

Participants

3

Reactant 2

HCID 6344DichloromethaneHCID 67412034HCID 67412034, compound

Product 1

HCID 67409996HCID 67409996, compound

Procedure

5-(2-fluoro-1,1-dimethyl-ethyl)-2-methyl-2H-pyrazole-3-carboxylic acid ethyl ester (722 mg, 3.16 mmol, prepared as described in the previous step) was dissolved in DCM (5 mL) and SO2Cl2 (0.256 mL, 3.16 mmol) was added dropwise to the stirred solution. The resulting mixture was stirred at room temperature for 16 h and then the solvent was removed under reduced pressure. The resulting residue was chromatographed on a 40-g SiO2 pre-packed column eluting with 0:1-1:4 EtOAc/heptane to yield 4-chloro-5-(2-fluoro-1,1-dimethyl-ethyl)-2-methyl-2H-pyrazole-3-carboxylic acid ethyl ester. 1H-NMR (400 MHz, CDCl3) δ: 4.59 (d, J=47 Hz, 2H), 4.40 (q, J=7.1 Hz, 2H), 4.08 (s, 3H), 1.43 (d, J=1.7 Hz, 6H), 1.41 (t, J=7.2 Hz, 3H).

Workup

  1. customthe solvent was removed under reduced pressure
  2. customThe resulting residue was chromatographed on a 40-g SiO2 pre-packed column
  3. washeluting with 0:1-1:4 EtOAc/heptane

Sources & evidence

ORD record
ord-6cfcdb730d524032876ca7526dea172d
Source dataset
uspto-grants-2015_05
Patent number
US09023846B2

Reaction notes

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