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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516807Generated: October 26, 2026

Diisopropylethylamine → 4-Bromo-N-(2-morpholin-4-ylethyl)thiophene-2-carboxamide

https://huagongshe.com/reaction/516807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-MorpholinoethylamineHCID 408285—
Reactant4-Bromo-2-Thiophenecarbonyl ChlorideHCID 2795483—
SolventDichloromethaneHCID 6344—
Product4-Bromo-N-(2-morpholin-4-ylethyl)thiophene-2-carboxamideHCID 23063724—

Reaction Steps

To a solution of 4-bromo-2-thiophenecarbonyl chloride (1.0 g, 4.4 mmol) in DCM (10 ml) cooled to 0° C. was added DIPEA (0.85 ml, 4.8 mml) and 4-(2-aminoethyl)morpholine (0.6 ml, 4.6 mmol) dropwise. Stirring was continued until complete consumption of the starting material was observed by LC-MS. The reaction was quenched by the addition of water, which was washed with further portions of 2N HCl, dried over sodium sulfate, filtered and concentrated in vacuo to yield the desired compound without need for further purification (1.6 g, 98%). δH (500 MHz, CHLOROFORM-d) 7.38 (1H, d, 1.3 Hz), 7.37 (1H, d, 1.1 Hz), 3.72-3.80 (4H, m), 3.53 (2H, q, 5.6 Hz), 2.59 (2H, t, 6.0 Hz), 2.48-2.54 (4H, m), TR=0.8 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115064B2
Source datasetuspto-grants-2015_08
ORD IDord-a24f56070fce4ebc975a0c9acf2aec59
Source noteuspto-grants-2015_08