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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061437Generated: November 1, 2026

HCID 66916106, compound → HCID 59205159, compound

https://huagongshe.com/reaction/2061437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66916106HCID 66916106—
ReactantHCID 86608852HCID 86608852—
SolventHydrochloric AcidHCID 313—
SolventIsopropanolHCID 3776—
ProductHCID 59205159HCID 59205159—

Reaction Steps

A solution of 6-Allyloxy-2-aminophenyl-sulfonamide (38 mg, 0.166 mmol) and 4-chloro-2-(3,4-dimethoxy-phenylamino)pyrimidine (44.2 mg, 0.166 mmol) in 2-propanol (5 ml) and 1N HCl (333 μl) is refluxed for 105 min. The reaction mixture is partitioned between ammonia (pH 10-11) and EtOAc. The organic layer is dried (Na2SO4) and concentrated. Precipitation with ether/hexanes gives the desired 2-Allyloxy-6-[2-(3,4-dimethoxy-phenylamino)-pyrimidin-4-ylamino]-benzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283356B2
Source datasetuspto-grants-2012_10
ORD IDord-160f2f43a16444a68410eb76b98df035
Source noteuspto-grants-2012_10