HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262247Generated: October 31, 2026
3-(Methylcarbamoyl)benzeneboronic acid → HCID 59593137, compound
https://huagongshe.com/reaction/2262247
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Methylcarbamoyl)benzeneboronic acid | HCID 2773524 | — |
| Reactant | 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole | HCID 45480186 | — |
| 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 59593137 | HCID 59593137 | — |
Reaction Steps
2-Chloro-6-iodo-7-methyl-4-morpholinothieno[3,2-d]pyrimidine from Example 12 (0.1 g, 0.3 mmol), 3-(N-Methylaminocarbonyl)benzeneboronic acid (50 mg, 0.3 mmol), and bis(triphenylphosphine)palladium(II) dichloride (9 mg, 13 μmol) in 1 M aqueous Na2CO3 (0.5 mL) and acetonitrile (0.5 mL) were heated to 100° C. in a sealed microwave reactor for 10 min. Upon completion, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole 7 (122 mg, 0.5 mmol), bis(triphenylphosphine)palladium(II) dichloride (9 mg, 13 μmol), 1 M aqueous Na2CO3 (1 mL), and acetonitrile (1 mL) 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 358 after reverse phase HPLC purification (2 mg). MS (Q1) 485 (M)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846929B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-adde83436b4240458779ef2716f72e18 |
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| Source note | uspto-grants-2010_12 |
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