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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589938Generated: October 30, 2026

Ammonia → HCID 117701113, compound

https://huagongshe.com/reaction/589938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPyridineHCID 1049—
ReactantTetrahydrofuranHCID 8028—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 117701113HCID 11770111392%

Reaction Steps

Carbonyldiimidazole (1.07 g, 6.60 mmol) was added to a tetrahydrofuran (15 mL) solution of the compound obtained in Reference Example 81 (1.03 g, 4.40 mmol) at room temperature, and the mixture was stirred at the same temperature for 40 minutes. A 28% aqueous ammonia solution (7 mL, excess amount) was added to the mixture at room temperature, and the resulting mixture was stirred at the same temperature for 20 minutes. Water was added to the reaction mixture, and the resulting mixture was extracted three times with ethyl acetate, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1→ethyl acetate, v/v). Subsequently, trifluoroacetic anhydride (0.612 mL, 4.40 mmol) was added to a methylene chloride (20 mL) solution of the compound thus obtained and pyridine (0.708 mL, 8.79 mmol) at 0° C., and the mixture was stirred at the same temperature for 20 minutes. Water and a saturated aqueous solution of ammonium chloride were added to the reaction mixture at 0° C., and the mixture was extracted three times with methylene chloride. The organic layer thus obtained was washed with water and a 1 M aqueous sodium hydroxide solution sequentially, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1→2:1, v/v) to give the title compound (867 mg, yield: 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233958B2
Source datasetuspto-grants-2016_01
ORD IDord-26f6ae239bdb491dbf98d3f5326828bf
Source noteuspto-grants-2016_01