HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098850Generated: November 1, 2026
3-(Methylsulfonyl)phenylboronic acid → HCID 59592895, compound
https://huagongshe.com/reaction/2098850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Methylsulfonyl)phenylboronic acid | HCID 2773542 | — |
| 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 59592895 | HCID 59592895 | — |
Reaction Steps
2-Chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-d]pyrimidine from Example 12 (0.3 g, 0.8 mmol), 3-(methylsulfonyl)phenylboronic acid (0.3 g, 1.5 mmol), and bis(triphenylphosphine)palladium(II) dichloride (30 mg, 40 μmmol) in 1 M aqueous Na2CO3 (1.5 mL) and acetonitrile (1.5 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 (0.4 g, 1.7 mmol), and bis(triphenylphosphine)palladium(II) dichloride (30 mg, 40 μmol) were added into the same pot. The reaction 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 395 after reverse phase HPLC purification (82 mg). MS (Q1) 506 (M)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450315B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-98a3c8e7be8448c381a2e84280bc9e2c |
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| Source note | uspto-grants-2013_05 |
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