HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxypteridin-2-amine → HCID 13235978, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxypteridin-2-amine | HCID 246283 | — |
| Reactant | HCID 11322793 | HCID 11322793 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13235978 | HCID 13235978 | 95% |
Reaction Steps
To a suspension of 0.88 g (0.005 mol) of 2-amino-4-methoxypteridine in 40 ml of absolute methylene chloride were added with stirring to 1.35 g (0.053 mol) of 2,2,2-trichloroethoxysulfonyl isocyanate. After about 10 minutes, a clear solution had formed and it was heated to reflux. After 10 minutes, the mixture was evaporated to dryness and the residue was treated with diisopropyl ether and a little acetone. The mixture was vacuum filtered and the product was dried to obtain 2.05 g (95% of theory) of N-(4-methoxypteridin-2-yl)-N'-(2,2,2-trichloroethoxysulfonyl)-urea in the form of yellow crystals melting at 93° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04509972 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-bba419f85335496c83fc0a8f5a04423b |
| Source note | uspto-grants-1985_04 |