HuagongsheHuagongshe Chemistry Print Report · For research reference only
[3-(2-morpholinoethoxy)phenyl]methylamine → HCID 24785532, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [3-(2-morpholinoethoxy)phenyl]methylamine | HCID 7164624 | — |
| Reactant | Methyl 5-(4-chlorophenyl)-3-(dimethylaminomethyleneamino)thiophene-2-carboxylate | HCID 11544322 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 24785532 | HCID 24785532 | — |
Reaction Steps
5-(4-Chlorophenyl)-3-(dimethylamino-methyleneamino)-thiophene-2-carboxylic acid methyl ester (0.164 g, 0.508 mmol), 3-(2-morpholin-4-yl-ethoxy)-benzylamine (0.100 g, 0.423 mmol) and MeOH (1.5 mL) were heated by MW at 120° C. for 15 minutes. The reaction mixture was allowed to cool to r.t., the precipitate filtered, washed with MeOH, and dried in vacuo to give the product. Yield: 0.110 g (45%). 1H NMR (400 MHz, CDCl3) δ 8.11 (s, 1H), 7.63 (d, 2H, J=8.42 Hz), 7.45 (s, 1H), 7.41 (d, 2H, J=8.42 Hz), 7.25 (m, 1H), 6.81-6.94 (m, 3H), 5.17 (s, 2H), 4.06 (t, 2H, J=6.12 Hz), 3.70 (t, 4H, J=4.68 Hz), 2.75 (t, 2H, J=5.58 Hz), 2.53 (t, 4H, J=4.51 Hz). MS (ESI+) 481.92 (M+1H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723331B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-10b371443b984ea7a063c718ca6412f0 |
| Source note | uspto-grants-2010_05 |