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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182212Generated: November 2, 2026

2-Morpholinoethylamine → HCID 86588190, compound

https://huagongshe.com/reaction/1182212

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MorpholinoethylamineHCID 408285—
ReactantHCID 1499213HCID 1499213—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
ProductHCID 86588190HCID 8658819060%

Reaction Steps

To a solution of N-aminoethylmorpholine (228 mg, 10 mmole) in 2 mL anhydrous THF at −40° C. was added 0.8 mL of 2 M n-BuLi solution in cyclohexane. Some white solid was precipitated instantly. The suspension was stirred for about a half an hour. When the bath temperature reached −10° C., a solution of 5-phenylamino-[1,2,3]thiadiazole-4-carboxylic acid ethyl ester (60 mg, 0.24 mmole) in anhydrous THF was added to the mixture. After it was stirred at room temperature for an hour, the reaction was quenched with saturated NH4Cl solution. The solution was extracted with EtOAc and residue obtained after the removal of EtOAc was purified by preparative TLC (silica gel, CH2Cl2:MeOH=15:1). The title compound was isolated as a white powder in 60% yield (48 mg). 1H NMR (ppm, in CDCl3): 10.91 (br. s, 1H), 7.77 (br. s, 1H), 7.00-7.60 (m, 5H), 3.70 (m, 4H), 2.60 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288556B2
Source datasetuspto-grants-2007_10
ORD IDord-0612473642a34ec799a3e9c0e45b053b
Source noteuspto-grants-2007_10