HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → 2-{[2-Aminoacetamido-5-chloro-alpha-(2-fluorophenyl)benzylidene]amino}ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Glycine Hydrochloride | HCID 22316 | — |
| Reactant | 2-{[2-Amino-5-chloro-alpha-(2-fluorophenyl)benzylidene]amino}ethanol | HCID 23322779 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-{[2-Aminoacetamido-5-chloro-alpha-(2-fluorophenyl)benzylidene]amino}ethanol | HCID 13341589 | 44.5% |
Reaction Steps
To a solution of 4.5g of N,N'-dicyclohexylcarbodiimide in 100ml of dimethylformamide is added a solution of 2.2g of glycine hydrochloride in 2.2ml of water in a period of about 30 seconds under stirring and ice-cooling. Immediately a solution of 3.2g of 2-{[2-amino-5-chloro-α-(2-fluorophenyl)benzylidene]amino}ethanol in 10ml of tetrahydrofuran is added dropwise to the above solution and the mixture is stirred for further 3 hours. After completion of the reaction, the reaction mixture is treated by the same manner as described in the Example 1, yielding 1.7g of the desired product melting at 128°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04022832 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-d46dc407160746ce91c68278008aa4d7 |
| Source note | uspto-grants-1977_05 |