HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661929Generated: November 1, 2026
Potassium Phosphate, Tribasic → HCID 59375021, compound
https://huagongshe.com/reaction/661929
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-(2-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)isoindolin-1-one | HCID 66606460 | — |
| Reactant | HCID 66606546 | HCID 66606546 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59375021 | HCID 59375021 | 58.9% |
Reaction Steps
A mixture of 5-bromo-2-(hydroxymethyl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide (Intermediate 30-3(a), 80 mg, 0.248 mmol), 2-(2-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)isoindolin-1-one (Intermediate 50-4, 130 mg, 0.371 mmol), 2 M aqueous tripotassium phosphate (0.371 mL, 0.743 mmol), and tetrakis(triphenylphosphine)palladium (14.30 mg, 0.012 mmol) in toluene (3 mL) and ethanol (1 mL) was sealed in a vial and heated at 100° C. for 6 hrs. The mixture was cooled and diluted with EtOAc, and the solution was washed with water, dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from DCM to 96:3.6:0.4 DCM-methanol-28% aqueous ammonium hydroxide) to provide 2-(hydroxymethyl)-5-(2-methyl-3-(1-oxoisoindolin-2-yl)phenyl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide as a light yellow solid (68 mg, 53%). 1H NMR (400 MHz, chloroform-d) δ 7.79 (1H, d, J=7.91 Hz), 7.46-7.53 (1H, m), 7.38-7.44 (2H, m), 7.30 (1H, dd, J=7.91, 3.08 Hz), 7.14-7.26 (3H, m), 6.77 (1H, dd, J=7.69, 2.86 Hz), 4.59-4.74 (2H, m), 3.39-3.54 (3H, m), 2.72-2.80 (2H, m), 2.30-2.44 (2H, m), 1.80-2.10 (3H, m), 1.75 (3H, d, J=8.35 Hz). Mass spectrum m/z 466.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084620B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-f44bc0ea59bd440eba3f46ce7d8b8a00 |
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| Source note | uspto-grants-2011_12 |
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