HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Cyclosulfamuron
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 2-Amino-4,6-dimethoxypyrimidine | HCID 118946 | — |
| Reactant | (2-Aminophenyl)(cyclopropyl)methanone | HCID 10931741 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Cyclosulfamuron | HCID 6451137 | — |
Reaction Steps
A solution of 1.78 g (0.0114 mole) of 2-amino-4,6-dimethoxypyrimidine in 50 mL of methylene chloride is cooled to 0.5° C. in an ice bath and 1.0 mL (1.62 g, 0.114 mole) of chlorosulfonyl isocyanate then added to the solution. The resulting mixture is stirred for 30 minutes and a solution of 2.66 g o-aminophenyl cyclopropyl ketone (70% real, 0.0114) and 2.6 mL triethylamine (0.0187 mole) in 50 mL of methylene chloride then slowly added to the mixture. The resulting solution is stirred at ambient temperature overnight (18 hours).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05009699 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-18d85f2360974f0eb021becd2f653f5a |
| Source note | uspto-grants-1991_04 |