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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358324Generated: October 25, 2026

Water → p-t-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamide

https://huagongshe.com/reaction/1358324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 15819130HCID 15819130—
ReactantHCID 131721323HCID 131721323—
SolventDimethyl SulfoxideHCID 679—
Productp-t-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamideHCID 15819129—

Reaction Steps

To a solution of 2 g of 4,6-dichloro-5-(o-methoxyphenoxy)-pyrimidine in 40 ml of DMSO 3.7 g of 4-tert.-butylbenzene sulfonamide potassium salt was added. The resulting solution was stirred for 20 h at room temperature. Eventually, the mixture was poured onto 400 ml of water and washed twice with 200 ml of diethyl ether. The organic layers was extracted with 200 ml of water. The combinded aqueous layers was acidified with conc. hydrochloric acid. The mixture was cooled to 0° C. and 100 ml of brine was added. The precipitate that formed was collected and dried to yield 2.7 g of 4-tert.-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]-benzene sulfonamide as a white powder. LC-MS: tR=5.80 min, [M+1]+=448.17, [M−1]−=446.21.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596719B1
Source datasetuspto-grants-2003_07
ORD IDord-9ef520da38ab408da4620f6240fa126c
Source noteuspto-grants-2003_07