HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262299Generated: November 1, 2026
Phenylboronic Acid → HCID 24969129, compound
https://huagongshe.com/reaction/2262299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo(2,3-b)pyridine | HCID 24208789 | — |
| Reactant | 2-Chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-d]pyrimidine | HCID 59592880 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | HCID 24969129 | HCID 24969129 | — |
Reaction Steps
2-Chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-d]pyrimidine from Example 12 (0.2 g, 0.5 mmol), phenylboronic acid (60 mg, 0.5 mmol), and bis(triphenylphosphine)palladium(II) dichloride (18 mg, 25 μmol) in 1 M aqueous Na2CO3 (1 mL) and acetonitrile (1 mL) were heated to 100° C. in a sealed microwave reactor for 10 min. Upon completion, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine (180 mg 0.75 mmol) and bis(triphenylphosphine)palladium(II) dichloride (13 mg, 20 μmol) were added and the mixture was heated to 150° C. in a sealed microwave reactor for 20 min. The mixture was extracted with EtOAc and CH2Cl2. The combined organics were concentrated to yield 420 after reverse phase HPLC purification (57 mg). MS (Q1) 428 (M)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07846929B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-3c9eb50f045b46e686ec7d8b4b0391fe |
|---|
| Source note | uspto-grants-2010_12 |
|---|