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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161639Generated: October 29, 2026

HCID 54687146, compound → HCID 54704003, compound

https://huagongshe.com/reaction/1161639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54687146HCID 54687146—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
ProductHCID 54704003HCID 5470400342%

Reaction Steps

7-iodosancycline, 150 mg (0.28 mM), Pd(OAc)2 and 10 mL of MeOH are added to a flask with a stir bar and the system degassed 3× using argon. Na2CO3 (87 mg, 0.8 mM) dissolved in water and argon degassed is added via syringe is added along with phenylboronic acid (68 mg, 0.55 mM) in MeOH that was also degassed. The reaction was followed by HPLC for 2 hours and cooled to room temperature. The solution was filtered, and dried to produce a crude mixture. The solid was dissolved in dimethylformamide and injected onto a preparative HPLC system using C18 reverse-phase silica. The fraction at 36-38 minutes was isolated, and the solvent removed in vacuo to yield the product plus salts. The salts were removed by extraction into 50:25:25 water, butanol, ethyl acetate and dried in vacuo. This solid was dissolved in MeOH and the HCl salt made by bubbling in HCl gas. The solvent was removed to produce the product in 42% yield as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820641B2
Source datasetuspto-grants-2010_10
ORD IDord-46017149a1b64d9bbdcadd29bdf4ae82
Source noteuspto-grants-2010_10