HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1'-Carbonyldiimidazole → Thalidomide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | N-Phthaloyl-L-glutamine | HCID 259136 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Thalidomide | HCID 5426 | 90% |
Reaction Steps
A stirred mixture of N-phthaloyl-L-glutamine (48.0 g, 174 mmoL), carbonyldiimidazole (30.43 g, 188 mmoL), and 4-dimethylaminopyridine (0.105 g, C.861 mmoL) in anhydrous tetrahydrofuran (300 mL) is heated to reflux for 16 hours. The reaction slurry is filtered and the solid washed with methylene chloride (200 mL). The solid is air-dried and then dried in vacuo (60° C.,<1 mm) to afford 40.40 g (90%) of thalidomide as a white powder. 1H NMR (DMSO-d6)δ 11.16 (s, 1H, NH), 8.05-7.80 (br s, 4H, Ar), 5.18 (dd, 1H, J=12, 5 Hz, CHCO), 3.05-2.85 (m, 1H, CH2CO), 2,70-2.45 (m, 2H, CH2CH2), 2.15-2.00 (M, 1H, CH2). 13C NMR (DMSO-d6)δ 172.8, 169.8, 167.1, 134.9, 131.2, 123.4, 49.0, 30.9, 22.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06075041 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-27a4e562c65d4a64a8f1c1da9fa8883e |
| Source note | uspto-grants-2000_06 |