p-Toluenesulfonic acid → HCID 71238321, compound

HRID 340070Notes

Reaction equation

[CH2:1]([C:3]1[CH:8]=[C:7]([O:9][CH3:10])[C:6]([F:11])=[CH:5][C:4]=1[C:12]1[CH:20]=[C:19]2[C:15]([C:16]([I:21])=[N:17][NH:18]2)=[CH:14][CH:13]=1)[CH3:2].CC1C=CC(S(O)(=O)=O)=CC=1.[O:33]1[CH:38]=[CH:37][CH2:36][CH2:35][CH2:34]1>C(Cl)Cl>[CH2:1]([C:3]1[CH:8]=[C:7]([O:9][CH3:10])[C:6]([F:11])=[CH:5][C:4]=1[C:12]1[CH:20]=[C:19]2[C:15]([C:16]([I:21])=[N:17][N:18]2[CH:34]2[CH2:35][CH2:36][CH2:37][CH2:38][O:33]2)=[CH:14][CH:13]=1)[CH3:2]

Participants

Conditions

Temperature: 0 °C

Procedure

To a solution of 6-(2-ethyl-5-fluoro-4-methoxy-phenyl)-3-iodo-1H-indazole (Preparation 16, 1.94 g, 4.9 mmol) in DCM (10 mL) was added p-TsOH (187 mg, 982 μmol) and the mixture was cooled to 0° C. 3,4-Dihydro-2H-pyran (660 μL, 7.4 mmol) was added dropwise to the solution and the reaction was stirred at room temperature overnight. The reaction mixture was diluted with DCM (5 mL) and washed with saturated sodium hydrogen carbonate aqueous solution (20 mL). The organic layer was dried over MgSO4 and concentrated in vacuo to yield a black oil. The residue was purified by column chromatography (Biotage SNAP 10 g) eluting with a gradient of 20% EtOAc in heptane to give the title compound as a colourless oil (2.09 g) in an 89% yield.

Workup

washwashed with saturated sodium hydrogen carbonate aqueous solution (20 mL)
dry with materialThe organic layer was dried over MgSO4
concentrationconcentrated in vacuo
customto yield a black oil
customThe residue was purified by column chromatography (Biotage SNAP 10 g)
washeluting with a gradient of 20% EtOAc in heptane

Sources & evidence

ORD record: ord-17cca2e45c7c4c87a653dddbb31cf9ed
Source dataset: uspto-grants-2014_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08895544B2

Reaction notes

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