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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722081Generated: October 31, 2026

1,1'-Carbonyldiimidazole → 5-Benzyl-2-(3-cyclopropyl-[1,2,4]oxadiazol-5-ylmethylsulfanyl)-pyrimidin-4-ylamine

https://huagongshe.com/reaction/722081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(4-Amino-5-benzyl-pyrimidin-2-ylsulfanyl)-acetic acidHCID 21883178—
ReactantHCID 178513214HCID 178513214—
SolventDimethylformamideHCID 6228—
Product5-Benzyl-2-(3-cyclopropyl-[1,2,4]oxadiazol-5-ylmethylsulfanyl)-pyrimidin-4-ylamineHCID 98810429%

Reaction Steps

A solution of (4-amino-5-benzyl-pyrimidin-2-ylsulfanyl)-acetic acid (0.35 mg, 1.27 mmol) as prepared according to the method described in example 22, and 1,1′-carbonyl-diimidazole (0.31 g, 1.91 mmol) in DMF (8 ml) was stirred at room temperature for 3 h and subsequently N-hydroxy-cyclopropanecarboxamidine (0.19 g, 1.91 mmol) was added. The reaction mixture was stirred at 80° C. for 20 h and evaporated. Acetic acid (10 ml) was added and the stirred mixture was heated under reflux conditions for 2 h. Aqueous work-up, column chromatography on silica gel (ethyl acetate/hexane 3:2) and crystallization from ethyl acetate/hexane yielded the title compound (36 mg, 9%) as an off-white solid, m.p. 94° C. and MS: m/e=340.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138404B2
Source datasetuspto-grants-2006_11
ORD IDord-c8a2dffda92146cdb0d4e4bf84002145
Source noteuspto-grants-2006_11