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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983097Generated: October 31, 2026

Methyl iodide → HCID 16722693, compound

https://huagongshe.com/reaction/1983097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 16722590HCID 16722590—
SolventDimethylformamideHCID 6228—
ProductHCID 16722693HCID 1672269358.4%

Reaction Steps

To a solution of cyclopropanecarboxylic acid {3-methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenyl}-amide (138 mg, 0.33 mmol) in DMF (2 mL) was added at ambient temperature potassium bis(trimethylsilyl)amide (0.91 M in THF, 0.44 mL, 0.40 mmol). After the dark brown solution was stirred for 15 min iodomethane (25 μL, 0.40 mmol) was added and the reaction mixture was stirred for 18 h in a closed flask. It was then extracted with water (20 mL) and ethyl acetate (20 mL). The combined organic layers were then washed with aqueous sodium carbonate (saturated, 20 mL), concentrated, dissolved in ethyl acetate (3 mL) and treated with heptane (3 mL). The resulting suspension was filtered off and washed with ethyl acetate:heptane 1:1 (3 mL) affording the title compound (83 mg, 58%) as a white solid. MS: m/e=431.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541372B2
Source datasetuspto-grants-2009_06
ORD IDord-489a1ae5f549474cb5d623df8940fd5d
Source noteuspto-grants-2009_06