HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642035Generated: October 30, 2026
HCID 54687146, compound → HCID 54704003, compound
https://huagongshe.com/reaction/1642035
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 54687146 | HCID 54687146 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | HCID 54704003 | HCID 54704003 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08119622B2 |
|---|
| Source dataset | uspto-grants-2012_02 |
|---|
| ORD ID | ord-824fa666df3e4b4597d48a29179f9399 |
|---|
| Source note | uspto-grants-2012_02 |
|---|