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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377945Generated: October 30, 2026

Triethylamine → HCID 59856891, compound

https://huagongshe.com/reaction/2377945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(-)-3-HydroxytetrahydrofuranHCID 641512—
Reactant4-(2-Fluoro-4-methanesulfonyl-phenoxy)-5-methyl-6-(piperidin-4-yloxy)-pyrimidineHCID 67202021—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59856891HCID 5985689142.9%

Reaction Steps

To a solution of 1,1′-carbonyldiimidazole (54.8 mg, 0.338 mmol) in 1 mL THF was added (R)-(+)-3-hydroxytetrahydrofuran (32 μl, 0.38 mmol). After stirring for 30 minutes at room temperature, 1 mL triethylamine, 1 mL THF, and 4-(2-fluoro-4-methanesulfonyl-phenoxy)-5-methyl-6-(piperidin-4-yloxy)-pyrimidine (70 mg, 0.166 mmol) were added. The resulting mixture was stirred at 60° C. for 48 hours and purified by HPLC to give Compound C177 as a white solid (35.3 mg, 42%). 1H NMR (CDCl3, 400 MHz) δ 1.81-1.88 (m, 2H), 1.96-2.09 (m, 3H), 2.12-2.20 (m, 4H), 3.10 (s, 3H), 3.42-3.48 (m, 2H), 3.75-3.81 (m, 2H), 3.84-3.97 (m, 4H), 5.27-5.31 (m, 1H), 5.34-5.38 (m, 1H), 7.41-7.45 (m, 1H), 7.77-7.82 (m, 2H), 8.20 (s, 1H). Exact mass calculated for C22H26FN3O7S 495.15, found 496.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470699B2
Source datasetuspto-grants-2008_12
ORD IDord-2b8e4bdcb10140218e108d34a0abc6fc
Source noteuspto-grants-2008_12