HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-[1-(2,4-Difluorobenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 1-(Chloromethyl)-2,4-difluorobenzene | HCID 2736948 | — |
| Reactant | 5-(Piperidin-4-ylmethoxy)quinazoline-2,4-diamine | HCID 57576565 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-[1-(2,4-Difluorobenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamine hydrochloride | HCID 25007783 | 78% |
Reaction Steps
The benzylamine was obtained by reacting 5-(piperidin-4-ylmethoxy)quinazoline-2,4-diamine (75 mg; 0.27 mmol) and 2,4-difluorobenzyl chloride (69 mg; 0.35 mmol) via Method BB. Solids were suspended in 2 mL dioxane and 0.5 mL 4M HCl in dioxane was added and after 2 hours stirring at room temperature solids were collected by filtration to yield 92 mg. (78% yield). 1HNMR (400 MHz, DMSO-d6) δ 12.8 (s, 1H), 11.2 (s, 1H), 8.84 (s, 1H), 8.23 (s, 1H), 7.88 (q, J=8.8, 6.4 Hz, 1H), 7.7 (m, 2H), 7.4 (m, 1H), 7.23 (m, 1H), 7.02 (m, 2H), 4.28 (d, J=4.4 Hz, 2H), 4.17 (d, J=6.4 Hz, 2H), 3.4 (br d, J=11.6 Hz, 2H), 2.95 (m, 2H), 2.23 (m, 1H), 1.81 (d, J=13.2 Hz, 2H), 1.73 (m, 2H). MS m/z (ESI) 400 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07985755B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-ce8ef275db1242e2a039b8cd76aa34c6 |
| Source note | uspto-grants-2011_07 |