HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245637Generated: October 25, 2026
9-Methoxy-9-borabicyclo(3.3.1)nonane → HCID 178498804, compound
https://huagongshe.com/reaction/245637
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 9-Methoxy-9-borabicyclo(3.3.1)nonane | HCID 544964 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Reactant | HCID 178498803 | HCID 178498803 | — |
| Catalyst | Bis(triphenylphosphine)palladium chloride | HCID 84124 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178498804 | HCID 178498804 | 66% |
Reaction Steps
To a solution of 899 mg (5.91 mmol) of 9-methoxy-9-bora-bicyclo[3.3.1]nonane in 5 mL of anhydrous tetrahydrofuran is added dropwise 3.71 mL (5.91 mmol) of a solution 1N of methyl lithium in diethylether. After few minutes of stirring, a mixture of 6-amino-3-bromo-5-chloro-1H-indazole-7-carboxylic acid methyl ester, prepared as in step a in example 39, and 104 mg (0.15 mmol) of bis(triphenylphosphine) palladiumI(II) dichloride in 10 mL of anhydrous tetrahydrofuran is added. The reaction mixture is stirred in a microwave oven at 150° C. for 15 minutes. After filtration over Celite and concentration in vacuo, the residue is purified by flash chromatography (SiO2, hexanes/ethyl acetate 1:1) to afford 470 mg of product (66%) as a pale yellowish solid; LC/MS:240/242 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658801B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-08bef5de52894447a2b63c14211b6865 |
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| Source note | uspto-grants-2014_02 |
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