HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
N-Methylbenzylamine → 5-[(Benzylmethylamino)methyl]-7-methyl-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-Methylbenzylamine | HCID 7669 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 5-Bromomethyl-7-methyl-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one | HCID 57949575 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 5-[(Benzylmethylamino)methyl]-7-methyl-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one | HCID 11662457 | 83% |
Reaktionsschritte
A solution of 5-bromomethyl-7-methyl-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one (50 mg, 0.12 mmol) in acetonitrile (3 mL) was added drop wise to N-methylbenzylamine (24 mg, 0.2 mmol) and diisopropylethylamine (0.17 mL, 1 mmol) in acetonitrile (5 mL). After 4 hours the reaction was evaporated. The residue was chromatographed on silica gel, eluting with 0 to 25% ethyl acetate in methylene chloride, to give 45 mg (83% yield) of 5-[(benzylmethylamino)methyl]-7-methyl-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one as a colorless oil. 1H NMR (300.132 MHz, CDCl3) δ 7.37-7.28 (m, 6H), 7.25-7.14 (m, 5H), 4.75 (s, 2H), 4.21 (s, 2H), 3.53 (s, 2H), 3.52 (s, 2H), 2.74 (s, 3H), 2.18 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07968570B2 |
| Quelldatensatz | uspto-grants-2011_06 |
| ORD ID | ord-405e7d0f34d041568e3518507383b78e |
| Quellennotiz | uspto-grants-2011_06 |