HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646587Generated: October 30, 2026
N,N-Diethylaniline → HCID 11369604, compound
https://huagongshe.com/reaction/646587
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Diethylaniline | HCID 7061 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178482629 | HCID 178482629 | — |
| Product | HCID 11369604 | HCID 11369604 | — |
Reaction Steps
A mixture of 7-(4-dimethylaminophenyl)-[1,6]naphthyridin-5-ol (Example 1) (1.2 g, 5 mmol), POCl3 (10 mL) and N,N-diethylaniline (0.15 g, 1.0 mmol) were stirred at 110° C. for 16 hours. The contents were cooled to room temperature and excess POCl3 was removed in vacuo. The residue was quenched with water and neutralized with aqueous sodium carbonate. The aqueous solution was then extracted with dichloromethane (2×30 mL). The combined organic extracts were dried over anhydrous magnesium sulfate and concentrated in vacuo to give a tan oil. Purification by flash chromatography eluting with hexanes/EtOAc (1:1) afforded the title compound as a yellowish solid (1.1 g). 1H NMR (CDCl3, 400 MHz) δ 9.03 (dd, 1H), 8.54 (d, 1H), 8.13 (s, 1H), 8.08 (d, 2H), 7.46 (dd, 1H), 6.81 (d, 2H), 3.05 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07705151B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-cd01e9fc89804e42a7357b697b983ba9 |
|---|
| Source note | uspto-grants-2010_04 |
|---|