HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-methoxy-5-(N-(2-morpholinoethyl)-methylsulfonamido)thiophene-2-carboxylic acid hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | ethyl 4-methoxy-5-(N-(2-morpholinoethyl)-methylsulfonamido)thiophene-2-carboxylate | HCID 86703862 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-methoxy-5-(N-(2-morpholinoethyl)-methylsulfonamido)thiophene-2-carboxylic acid hydrochloride | HCID 86703863 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a solution of ethyl 4-methoxy-5-(N-(2-morpholinoethyl)-methylsulfonamido)-thiophene-2-carboxylate (Int. 70, 375 mg, 0.955 mmol) (prepared as described in Step 6 hereabove reported) in dioxane (8 ml), aqueous 37% HCl (3 ml) was added drop wise, and the resulting mixture was heated under MW irradiation at 100° C. for 3.5 hours. The volatiles were removed under vacuum to afford 4-methoxy-5-(N-(2-morpholinoethyl)-methylsulfonamido)thiophene-2-carboxylic acid hydrochloride (Int. 71) (383 mg, 0.955 mmol, MS/ESI+364.9 [MH]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440954B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-13d8149d02f44a0abbccd76f0b249bb4 |
| Source note | uspto-grants-2016_09 |