HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propargylaminoacetaldehyde → 2-[1-Propargyl-3-(7-bromobenzothiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propargylaminoacetaldehyde | HCID 20392754 | — |
| Reactant | 7-Bromobenzothiazol-2-yl isocyanate | HCID 53646458 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[1-Propargyl-3-(7-bromobenzothiazol-2-yl)ureido]acetaldehyde | HCID 20357136 | — |
Reaction Steps
7-Bromobenzothiazol-2-yl isocyanate dimer (0.1 mole), the dimethyl acetal of 2-propargylaminoacetaldehyde (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-propargyl-3-(7-bromobenzothiazol-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-afb96df029134a9992980bcd0aa1bb36 |
| Source note | uspto-grants-1977_06 |