HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenesulfonyl chloride → Methyl 5-methyl-4-[(2-thienylsulfonyl)amino]thiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenesulfonyl chloride | HCID 85518 | — |
| Reactant | Methyl 4-amino-5-methylthiophene-2-carboxylate | HCID 59640747 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Methyl 5-methyl-4-[(2-thienylsulfonyl)amino]thiophene-2-carboxylate | HCID 59411395 | 96.3% |
Reaction Steps
To a mixture of methyl 4-amino-5-methylthiophene-2-carboxylate (20 g) and pyridine (100 mL) was added 2-thiophen-sulfonyl chloride (23.5 g) at 0° C., and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, water was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography to give methyl 5-methyl-4-[(2-thienylsulfonyl)amino]thiophene-2-carboxylate (35.7 g, yield 96%) as pale-yellow crystals from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492405B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-f98ef8475d544d2f9dc0ff43e6baba46 |
| Source note | uspto-grants-2013_07 |