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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058106Generated: November 2, 2026

Sodium Hydroxide → Methyl [6-methyl-2-[(2-thienylsulfonyl)aminocarbonylamino]pyrimidin-4-yloxy]acetate

https://huagongshe.com/reaction/2058106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantThiophene-2-sulfonyl isocyanateHCID 12875192—
ReactantMethyl (2-amino-6-methylpyrimidin-4-yloxy)acetateHCID 13469547—
SolventDichloromethaneHCID 6344—
ProductMethyl [6-methyl-2-[(2-thienylsulfonyl)aminocarbonylamino]pyrimidin-4-yloxy]acetateHCID 13469548—

Reaction Steps

To a dry stirred solution of 18 parts of methyl (2-amino-6-methylpyrimidin-4-yloxy)acetate in 300 parts of methylene chloride at ambient temperature was added 20 parts of 2-thiophenesulfonylisocyanate. The solution was allowed to stand for 3 hours and was then poured onto ice. The pH of the aqueous layer was adjusted to 11 with sodium hydroxide solution and the methylene chloride layer was separated therefrom. The aqueous layer was neutralized with aqueous hydrochloric acid and then extracted with methylene chloride. The extract was dried and stripped of solvent to yield 8 parts of methyl [6-methyl-2-[(2-thienylsulfonyl)aminocarbonylamino]pyrimidin-4-yloxy]acetate, m.p. 114°-120°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04214890
Source datasetuspto-grants-1980_07
ORD IDord-c4643307161a41b7af31aec0d5bdcde2
Source noteuspto-grants-1980_07