Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-Chloro-2-methoxyphenylboronic acid | HCID 2735751 | — |
| Reactant | N-(7-bromoisoquinolin-3-yl)cyclopropanecarboxamide | HCID 67974626 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67974827 | HCID 67974827 | 10.2% |
Reaction Steps
N-(7-bromoisoquinolin-3-yl)cyclopropanecarboxamide (150 mg, 0.595 mmol), 5-chloro-2-methoxyphenylboronic acid (132 mg, 0.714 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (24 mg, 0.03 mmol) and cesium carbonate (232 mg, 0.714 mmol) were mixed in acetonitrile and water (10:1, 20 mL). The reaction mixture was stirred at 120° C. under nitrogen for 6 hours. The reaction mixture was concentrated, diluted with water and extracted with ethyl acetate, concentrated and purified by prep-HPLC to give the desired product (21.3 mg, 10.2%). LCMS (ESI): RT (min)=1.216, M+H+=352.9, Method=I; 1H NMR (400 MHz, DMSO-d6) δ 10.93 (s, 1H), 9.14 (s, 1H), 8.46 (s, 1H), 8.12 (s, 1H), 7.84-7.42 (m, 4H), 7.18 (d, J=8.4 Hz, 1H), 3.78 (s, 3H), 2.09-2.05 (m, 1H), 0.88-0.83 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206175B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-431467ae5a514c5baa77164ad063dc0b |
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| Source note | uspto-grants-2015_12 |
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