HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloromethylaminoacetaldehyde → 2-[1-Chloromethyl-3-(5-fluorobenzothiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloromethylaminoacetaldehyde | HCID 20392716 | — |
| Reactant | 5-Fluorobenzothiazol-2-yl isocyanate | HCID 45077455 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[1-Chloromethyl-3-(5-fluorobenzothiazol-2-yl)ureido]acetaldehyde | HCID 20357124 | — |
Reaction Steps
5-Fluorobenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-chloromethylaminoacetaldehyde (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 one 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-chloromethyl-3-(5-fluorobenzothiazol-2-yl)ureido]acetaldehyde as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04029491 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-b77cc0dfb1784e9f96535ae8601df951 |
| Source note | uspto-grants-1977_06 |