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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163070Generated: October 28, 2026

Potassium Carbonate → N-(3-(4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)propyl)methanesulfonamide

https://huagongshe.com/reaction/1163070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-fluoro-2-methyl-1H-indol-5-olHCID 10352036—
ReactantHCID 178431435HCID 178431435—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-(3-(4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)propyl)methanesulfonamideHCID 1160476336.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-[3-(4-hydroxy-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)-propyl]-methanesulfonamide (530 mg, 1.77 mmol) and POCl3 was heated at 80° C. for 1.5 h. The volatiles were removed and the residue was diluted with dichloromethane, washed successively with cold NaHCO3 solution and brine, dried, and concentrated in vacuo to afford the crude chloroimidate intermediate (610 mg), which was heated with 4-fluoro-2-methyl-1H-indol-5-ol (495 mg, 3.0 mmol) and K2CO3 (3.0 g, 22 mmol) in DMF (8 mL) at 80-85° C. for 2 h. The mixture was diluted with dichloromethane and the solid was filtered. The filtrate was concentrated and the residue was purified by silica gel flash column chromatography eluting with 30% ethyl acetate/dichloromethane. The desired product was further purified by preparative HPLC to afford the title compound (290 mg, 34% yield) as a tan solid. HRMS (M+H)+ Calcd. For C20H22FN5O4S: 447.1376. Found: 448.1476. 1H NMR (CDCl3) δ7.75 (s, 1H), 7.24 (s, 1H), 7.03 (d, 1H, J=8.32 Hz), 6.88 (m, 1H), 4.04 (t, 2H, J=5.72 Hz), 3.31 (t, 2H, J=6.16 Hz), 2.90 (s, 3H), 2.42 (s, 3H), 2.37 (s, 3H), 2.04 (m, 2H). Anal. Calcd. For C20H21FN4O4S: 1.0H2O:0.18 TFA: C, 50.57; H, 4.73; N, 14.61; S 6.80. Found: C, 50.44; H, 4.87; N, 14.51; S 6.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820814B2
Source datasetuspto-grants-2010_10
ORD IDord-f50556eb89cb4d0ca4875c6bc7b39e7d
Source noteuspto-grants-2010_10