HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonic acid → 5-(2-Acetamido-4-methylthiazol-5-yl)furan-2-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | N-(5-(furan-2-yl)-4-methylthiazol-2-yl)acetamide | HCID 59362180 | — |
| Product | 5-(2-Acetamido-4-methylthiazol-5-yl)furan-2-sulfonyl chloride | HCID 59362176 | — |
Reaction Steps
To N-(5-(furan-2-yl)-4-methylthiazol-2-yl)acetamide (0.443 g) under an ice-salt bath was added sulfurochloridoic acid (ClSO3H, 5 ml). After 30 min, the reaction was poured into crushed ice (150 g). Extraction with dichloromethane (3×30 ml), drying and concentration gave 5-(2-acetamido-4-methylthiazol-5-yl)furan-2-sulfonyl chloride (0.359 g) that was used directly for next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268818B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-0c5e5284cfa54de9a260e7292472f86f |
| Source note | uspto-grants-2012_09 |