HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Methylsulfonylthiazol-2-yl isocyanate → 2-[1-beta-Bromoethyl-3-(5-methylsulfonylthiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Methylsulfonylthiazol-2-yl isocyanate | HCID 54056032 | — |
| Reactant | HCID 54272806 | HCID 54272806 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[1-beta-Bromoethyl-3-(5-methylsulfonylthiazol-2-yl)ureido]acetaldehyde | HCID 53818112 | — |
Reaction Steps
5-Methylsulfonylthiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-β-bromoethylaminoacetaldehyde (0.2 mole) and benzene (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is stirred at ambient temperatures for a period of about 1 hour. After this time the reaction mixture is filtered, and the filtrate is stripped of solvent to yield the desired product the dimethyl acetal of 2-[1-β-bromoethyl-3-(5-methylsulfonylthiazol-2-yl)ureido]acetaldehyde as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04097485 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-21731131c92b4c1c8eb103892e558e39 |
| Source note | uspto-grants-1978_06 |