Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | HCID 58169400 | HCID 58169400 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 50943451 | HCID 50943451 | 28.1% |
Reaction Steps
A mixture of 2-bromo-N-(5-cyclopropyl-1H-pyrazol-3-yl)-5-fluoropyrimidin-4-amine (250 mg, 0.84 mmol, 1.0 eq), thiophen-2-ylboronic acid (150 mg, 1.18 mmol, 1.4 eq), Pd(dppf)Cl2 (69 mg, 0.084 mmol, 0.1 eq), Na2CO3 (356 mg, 3.36 mmol, 4 eq), 1,4-dioxane (10 ml) and water (1.5 ml) was stirred at 100° C. under a nitrogen atmosphere for 15 h. The reaction mixture was allowed to cool to room temperature and concentrated to give a residue. The residue was purified by silica gel chromatography (CH2Cl2/methanol 500:1 to 100:1 as eluent) to afford title compound N-(5-cyclopropyl-1H-pyrazol-3-yl)-5-fluoro-2-(thiophen-2-yl)pyrimidin-4-amine (Compound 41) (71.2 mg, 28.1%) as a solid. LC-MS (m/z)=302.1 [M+H]+; 1H NMR (400 MHz, DMSO-d6): δ 0.77 (d, J=4 Hz, 2H), 1.01 (d, J=7.2 Hz, 2H), 1.97 (t, J=4.4 Hz, 1H), 6.58 (s, 1H), 7.21 (t, J=4.2 Hz, 1H), 7.76 (m, 2H), 8.32 (d, J=3.2 Hz, 1H), 10.12 (s, 1H), 12.24 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422271B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-f1f8bac22b4243a4bd495c23ffb6bcf7 |
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| Source note | uspto-grants-2016_08 |
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