HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 4-Bromo-N-(2-morpholin-4-ylethyl)thiophene-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Morpholinoethylamine | HCID 408285 | — |
| Reactant | 4-Bromo-2-Thiophenecarbonyl Chloride | HCID 2795483 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-N-(2-morpholin-4-ylethyl)thiophene-2-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115064B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-a24f56070fce4ebc975a0c9acf2aec59 |
| Source note | uspto-grants-2015_08 |