HuagongsheHuagongshe Chemistry Print Report · For research reference only
B-[2-(1-Piperazinyl)-4-pyridinyl]boronic acid → HCID 46871653, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | B-[2-(1-Piperazinyl)-4-pyridinyl]boronic acid | HCID 53443448 | — |
| Reactant | 1-(5-Chloro-2-trifluoromethylbenzyl)-7-iodo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine | HCID 57886085 | — |
| Product | HCID 46871653 | HCID 46871653 | — |
Reaction Steps
1-[5-Chloro-2-(trifluoromethyl)benzyl]-7-iodo-1,2,3,4-tetrahydro-pyrido[2,3-b]pyrazine (293 mg) was reacted with 2-(piperazin-1-yl)pyridine-4-boronic acid, pinacol ester as in General Procedure 4B to give the title compound as an off-white solid. m.p.=189° C., LCMS: m/z=489.08 (M+H+), 1H-NMR (CDCl3, 400 MHz) δ 2.98 (4H, m), 3.49 (6H, m), 3.71 (2H, m), 4.61 (2H, s), 5.29 (1H, s), 5.34 (1H, bs), 6.55 (2H, m), 6.64 (1H, dd, J=5.2, 1.4 Hz), 7.36 (1H, d, J=8.1 Hz), 7.52 (1H, s), 7.64 (1H, d, J=8.3 Hz), 7.77 (1H, d, J=2.0 Hz), 8.12 (1H, d, J=5.3 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08080561B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-2fbced28a8ad4db4ac95060195198b7e |
| Source note | uspto-grants-2011_12 |