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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252734Generated: October 25, 2026

Citric Acid → Ethanesulfonic acid [6-[2-(5-methylsulfanyl-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amide

https://huagongshe.com/reaction/2252734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-5-(methylthio)pyrimidineHCID 21979532—
ReactantEthanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2]bipyrimidinyl-4-yl]-amideHCID 59645268—
SolventTetrahydrofuranHCID 8028—
ProductEthanesulfonic acid [6-[2-(5-methylsulfanyl-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amideHCID 5964527651%

Reaction Conditions

Temperature75 °C

Reaction Steps

Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (89 mg) was dissolved in THF (6 ml). Sodium hydride (40 mg) and 2-chloro-5-methylsulfanyl-pyrimidine (71 mg) were added and the mixture was heated to 75° C. for 48 h, then poured onto water, acidified with solid citric acid and the precipitate was filtered off. The crude material was purified by crystallization from methanol to give ethanesulfonic acid [6-[2-(5-methylsulfanyl-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (58 mg) as a white powder. LC-MS: tR: 4.15, [M+H]+: 572.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323465B2
Source datasetuspto-grants-2008_01
ORD IDord-3366eef3f8e94ef1a28a12fce94c725a
Source noteuspto-grants-2008_01