HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 59369649, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenepropanoyl chloride | HCID 64801 | — |
| Reactant | 2-Amino-4-morpholin-4-ylmethylthiazole-5-carboxylic acid benzylamide | HCID 86642523 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59369649 | HCID 59369649 | 74.1% |
Reaction Steps
To a solution of 2-amino-4-morpholin-4-ylmethylthiazole-5-carboxylic acid benzylamide (0.030 g, 0.09 mmol) in tetrahydrofuran (5 mL) at 0° C. was added hydrocinnamoyl chloride (0.1 mL, 0.67 mmol), 4-dimethylaminopyridine (catalytical amount) and triethylamine (0.2 mL, 1.4 mmol). The reaction mixture was allowed to warm to ambient temperature over 18 h then concentrated in vacuo. The crude product was purified by flash column chromatography eluting with ethyl acetate/hexanes (5/95 to 100/0) to afford the title compound (0.031 g); 1H NMR (DMSO-d6, 400 MHz) δ 7.40-7.15 (m, 10H), 4.46 (d, J=5.1 Hz, 2H), 3.62 (s, 2H), 3.19 (bs, 4H), 2.91 (t, J=7.6 Hz, 2H), 2.74 (t, J=8.1 Hz, 2H), 2.24 (br, s, 4H); MS (ES+) m/z 465 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541457B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-fc9dc78fab284c02b4fa0fec7a35e31b |
| Source note | uspto-grants-2013_09 |