HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 131735243, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2-Chloropyrimidin-5-yl)boronic acid | HCID 21747362 | — |
| Reactant | (4-Methylpiperidin-4-yl)methanol--hydrogen chloride (1/1) | HCID 66653509 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131735243 | HCID 131735243 | — |
Reaction Steps
(4-Methylpiperidin-4-yl)methanol hydrochloride (2.09 g, 12.63 mmol), (2-chloropyrimidin-5-yl)boronic acid (2 g, 12.63 mmol) and triethylamine (1.8 mL, 12.630 mmol) in ethanol (15 mL) was stirred at 80° C. overnight. The reaction mixture was cooled to r.t. and concentrated in vacuo to give the title compound as an orange semi-solid. This material was used without any further purification. HPLC-MS: MH+ m/z 252.2, RT 0.34 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309243B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-cb46d7070ce545c28b272879d4b6b3bf |
| Source note | uspto-grants-2016_04 |