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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642035Generated: October 30, 2026

HCID 54687146, compound → HCID 54704003, compound

https://huagongshe.com/reaction/1642035

Reaction equation

Participants

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

Reaction Steps

7-iodosancycline, 150 mg (0.28 mM), Pd(OAc)2 and 10 mL of Me0H 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 Me0H 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 before extraction into 50:25:25 water:butanol:ethyl acetate and dried in vacuo. This solid was dissolved in Me0H and the HCl salt made by bubbling in HCl gas. The solvent was removed to produce the product, substantially free of positional isomers, in 42% yield as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119622B2
Source datasetuspto-grants-2012_02
ORD IDord-824fa666df3e4b4597d48a29179f9399
Source noteuspto-grants-2012_02