HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012178Generated: October 29, 2026
2,6-Dimethylphenylboronic acid → 3-{4-[5-(2,6-Dimethylphenyl)-thiophen-2-yl]-pyrimidin-2-ylamino}-phenylethanol
https://huagongshe.com/reaction/1012178
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dimethylphenylboronic acid | HCID 583322 | — |
| Reactant | HCID 16666603 | HCID 16666603 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-{4-[5-(2,6-Dimethylphenyl)-thiophen-2-yl]-pyrimidin-2-ylamino}-phenylethanol | HCID 16666646 | 30.5% |
Reaction Steps
1-{3-[4-(5-Bromothiophen-2-yl)pyrimidin-2-ylamino]-phenyl}-ethanol (15 mg, 0.04 mmol), 2,6-dimethlphenylboronic acid (7.2 mg, 0.048 mmol) and PdCl2(dppf)2 (1.6 mg, 0.002 mmol) were combined in Smith microwave vial (0.2-5.0 mL) in degassed DMA (300 uL) and 2 M Na2CO3 (250 uL). The mixture was micro waved at 165° C. for 900 s. The mixture was diluted with 500 uL DMSO and purified directly by preparative HPLC to afford 1-(3-{4-[5-(2,6-dimethylphenyl)-thiophen-2-yl]-pyrimidin-2-ylamino}-phenylethanol (4.9 mg, 30% yield). 1H NMR (500 MHz, DMSO-d6) δ 1.29 (d, J=6.5 Hz, 3H), 2.14 (s, 6H), 4.64 (m, 1H), 5.07 (d, J=3.5 Hz, 1H), 6.91 (d, J=8 Hz, 1H), 7.02 (d, J=4 Hz, 1H), 7.16-7.25 (m, 4H), 7.35 (d, J=5 Hz, 1H), 7.60 (d, J=8 Hz, 1H), 7.84 (br t, 1H), 8.03 (d, J=3.5 Hz, 1H), 8.48 (d, J=5 Hz, 1H), 9.58 (s, 1H). MS: m/z 402 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977481B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-24187921ad6a423b932fe35b2953a0c7 |
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| Source note | uspto-grants-2011_07 |
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