Water → 3-Methoxypropyl indazole amide

HRID 2054340Notes

Reaction equation

[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([C:10]([NH2:12])=[O:11])=[N:2]1.Br[CH2:14][CH2:15][CH2:16][O:17][CH3:18].[H-].[Na+].O>CN(C=O)C>[CH3:18][O:17][CH2:16][CH2:15][CH2:14][C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:4]=1[C:3]([C:10]([NH2:12])=[O:11])=[N:2][NH:1]2

Participants

Conditions

Temperature: 60 °C

Procedure

Following the procedure for converting Compound 1e to Compound 1f, the indazole amide Compound 1e (0.31 g, 17.8 mmol) was treated with 1-bromo-3-methoxypropane (0.3 g, 19.6 mmol) in the presence of 95% NaH (0.05 g, 19.6 mmol) in DMF (50 mL) at 0° C. for 20 min and then warmed to 60° C. for 2 h. The mixture was cooled down to rt. Water was added and the aqueous solution was extracted with EtOAc several times. The organic layers were combined and washed with brine, then dried (Na2SO4) and evaporated in vacuo to an oil. The oil was purified by flash column chromatography (96:4:0.4; DCM:MeOH:NH4OH) to afford a 3-methoxypropyl indazole amide analog of Compound 1f (0.32 g, 73%). 1H NMR (CDCl3) δ 7.69 (d, J=8.13 Hz, 1H), 7.4 (m, 2H), 7.17 (m, 1H), 6.57 (bd s, 1H), 5.39 (bd s, 1H), 4.47 (t, J=6.65 Hz, 2H), 3.96 (s, 2H), 3.30 (t, J=5.78 Hz, 2H), 3.28 (s, 3H), 2.16 (m, 2H). ES-MS m/z 248 (MH+).

Workup

temperatureThe mixture was cooled down to rt
extractionthe aqueous solution was extracted with EtOAc several times
washwashed with brine
dry with materialdried (Na2SO4)
customevaporated in vacuo to an oil
customThe oil was purified by flash column chromatography (96:4:0.4; DCM:MeOH:NH4OH)

Sources & evidence

ORD record: ord-85d7a8eb42d444a7b40516dd14fc3f0c
Source dataset: uspto-grants-2008_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07329657B2

Reaction notes

Loading…