HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chlorothiophene-2-sulfonyl isoleucinol → 5-Chloro-N-[(S,S)-1-formyl-2-methylbutyl]thiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chlorothiophene-2-sulfonyl isoleucinol | HCID 9879302 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Chloro-N-[(S,S)-1-formyl-2-methylbutyl]thiophene-2-sulfonamide | HCID 59086201 | 81.2% |
Reaction Steps
Molecular sieves (15 g, 4 Å) were stirred in dry CH2Cl2 (175 mL) for 10 min. Then a mixture of pyridinium chlorochromate (8.6 g, 39.9 mmol) and silica gel (9 g) was added and the mixture was stirred an additional 10 min. To the suspension was added 5-chlorothiophene-2-sulfonyl isoleucinol (4 g, 13.4 mmol) dissolved in CH2Cl2 (15 mL) and the resulting slurry was stirred for 2 h. The reaction mixture was filtered and the solvent was removed. The residue was subjected to a Biotage™ eluting with 20% EtOAc/hexane to give 3.22 g (81%) of the aldehyde (LCMS=294.21 (M−H), rt=1.10 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06610734B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-bc3948bc8269481286914b7f901385b5 |
| Source note | uspto-grants-2003_08 |