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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980446Generated: November 1, 2026

4-Methoxypteridin-2-amine → HCID 13235978, compound

https://huagongshe.com/reaction/1980446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxypteridin-2-amineHCID 246283—
ReactantHCID 11322793HCID 11322793—
SolventDichloromethaneHCID 6344—
ProductHCID 13235978HCID 1323597895%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04509972
Source datasetuspto-grants-1985_04
ORD IDord-bba419f85335496c83fc0a8f5a04423b
Source noteuspto-grants-1985_04