HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983100Generated: October 31, 2026
Bromomethylcyclopropane → HCID 67215162, compound
https://huagongshe.com/reaction/1983100
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 3-Methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenylamine | HCID 16722587 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67215162 | HCID 67215162 | 12.2% |
Reaction Steps
To a suspension of 3-methoxy-4-[5-(5-methyl-3-phenyl-isoxazol-4-yl)-[1,3,4]oxadiazol-2-yl]-phenylamine (200 mg, 0.57 mmol) in THF were added N,N-diisopropyl ethyl amine (128 μL, 0.75 mmol) and bromomethyl-cyclopropane (61 μL, 0.63 mmol) and the reaction mixture was stirred for 24 h at ambient temperature. After addition of potassium bis(trimethylsilyl)amide (0.91 M in THF, 0.82 mL, 0.75 mmol) was added stirring was continued for 15 min and further bromomethyl-cyclopropane (78 μL, 0.80 mmol) was added. After stirring for 18 h at ambient temperature further bromomethyl-cyclopropane (0.12 mL, 1.2 mmol) was added and stirring continued for 24 h at this temperature. The reaction mixture was extracted with aqueous sodium carbonate (saturated, 20 mL) and ethyl acetate (20 mL). The aqueous layer was extracted with ethyl acetate (20 mL) and the combined organic layers dried over sodium sulfate. Concentration and then purification by chromatography (SiO2, heptane:ethyl acetate:dichloromethane=40:40:20 to 0:80:20) afforded the title compound (28 mg, 12%) as a light brown solid. MS: m/e=403.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07541372B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-140030926a79409ea4f3757b35c8de26 |
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| Source note | uspto-grants-2009_06 |
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