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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671781Generated: November 3, 2026

2-Morpholinoethylamine → HCID 15940239, compound

https://huagongshe.com/reaction/1671781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MorpholinoethylamineHCID 408285—
ReactantHCID 57527166HCID 57527166—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15940239HCID 1594023954%

Reaction Steps

A solution of 2-bromo-6-(4-(4-fluorophenyl)oxazol-5-yl)benzo[d]thiazole (0.030 g, 0.080 mmol, 1.0 eq.) and 4-(2-aminoethyl)morpholine (0.073 mL, 0.556 mmol, 7.0 eq.) in THF (1.5 mL) was mechanically shaken at 54° C. overnight. After cooling to room temperature, the solution was concentrated in vacuo. MeOH was added to the residue, and the mixture was subjected to autoprep. The appropriate fractions were collected, and NaHCO3 (s) was added. The solution was then concentrated in vacuo not to dryness and extracted with CH2Cl2 (3×). The organic layers were combined, dried over Na2SO4, filtered, and concentrated in vacuo to give 6-(4-(4-fluorophenyl)oxazol-5-yl)-N-(2-morpholinoethyl)benzo[d]thiazol-2-amine as a light yellow solid (0.0182 g, 54% yield). LC/MS (MH)=425.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994337B2
Source datasetuspto-grants-2011_08
ORD IDord-28a5cd0a3b6f4ae381a618265dd49298
Source noteuspto-grants-2011_08