HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → N-(3-(thiazol-2-ylamino)phenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | N-(3-thioureidophenyl)methanesulfonamide | HCID 86674185 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(3-(thiazol-2-ylamino)phenyl)methanesulfonamide | HCID 86674184 | 93.4% |
Reaction Steps
N-(3-thioureidophenyl)methanesulfonamide 54 (1.14 g, 4.65 mmol) and 50% aq. chloroacetaldehyde solution (3.65 mL, 23.25 mmol) were taken into ethanol and refluxed for 2 hours. Reaction mixture was concentrated and aq. Saturated NaHCO3 was added. Resulting light brown solid was filtered and washed with water, dried under high vacuum to obtain N-(3-(thiazol-2-ylamino)phenyl)methanesulfonamide 55 (1.17 g, 93% yield). Resulting product was further used without further purification. MS (ES) m/z 270 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08865709B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-22d29d370b464ea9be57fe2479bb1a6e |
| Source note | uspto-grants-2014_10 |