HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78538Generated: November 2, 2026
Dichloromethane → 5-methyl-3-(2-morpholinoethyl)thiazol-2(3H)-imine
https://huagongshe.com/reaction/78538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| Reactant | 2-Amino-5-methylthiazole | HCID 351770 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | 5-methyl-3-(2-morpholinoethyl)thiazol-2(3H)-imine | HCID 68623414 | 88.6% |
Reaction Steps
A mixture of 2-amino-5-methylthiazole (1.0 g, 8.8 mmol), 4-(2-chloroethyl)-morpholine hydrochloride (1.7 g, 9.2 mmol) and Et3N (3.7 mL, 26 mmol) in DMF (5 mL) was warmed to 80° C. and was allowed to stir for 24 h. The mixture was then cooled to ambient temperature, quenched with saturated aqueous NaHCO3 (5 mL), and diluted with CH2Cl2 (5 mL). The layers were separated and the aqueous layer was extracted with CH2Cl2 (3×5 mL). The combined organics were dried over anhydrous Na2SO4, filtered, concentrated under reduced pressure and purified via column chromatography (SiO2, 10% CH3OH in EtOAc then 9:1:0.1 CH2Cl2:CH3OH:NH4OH) to give the title compound (0.88 g, 3.9 mmol, 44% yield). MS (DCI/NH3) m/z 228 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08841334B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-1e19bda0b23f4a049223573c0023ef3a |
|---|
| Source note | uspto-grants-2014_09 |
|---|