HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59745Generated: October 29, 2026
Potassium Carbonate → methyl 3-(N-(2-morpholinoethyl)-methylsulfonamido)thiophene-2-carboxylate
https://huagongshe.com/reaction/59745
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| Reactant | Methyl 3-[(methylsulfonyl)amino]-2-thiophenecarboxylate | HCID 2820039 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 3-(N-(2-morpholinoethyl)-methylsulfonamido)thiophene-2-carboxylate | HCID 86703849 | — |
Reaction Steps
A mixture of methyl 3-(methylsulfonamido)thiophene-2-carboxylate (prepared in an analogous manner as described in Example 8, Scheme 8, Step 1, 500 mg, 2.125 mmol), 4-(2-chloroethyl)morpholine hydrochloride (435 mg, 2.338 mmol) and potassium carbonate (646 mg, 4.68 mmol) in dry DMF (13 ml) was heated at 80° C. for 5 h and stirred at RT for 3 days. The solvent was evaporated, the residue was diluted with EtOAc and washed with H2O and brine; the organic layer was dried over Na2SO4, filtered and evaporated. The crude was purified by flash chromatography on silica gel (DCM/EtOAc=8/2 to 7/3 and then DCM/MeOH=95/5) to afford methyl 3-(N-(2-morpholinoethyl)-methylsulfonamido)thiophene-2-carboxylate (Int. 50) (655 mg, 1.880 mmol, MS/ESI+ 348.9 [MH]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440954B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-6e8217b4537d4cc2a66651400d30ac80 |
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| Source note | uspto-grants-2016_09 |
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