HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hippuric Acid → HCID 14626423, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hippuric Acid | HCID 464 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Dibenzyl L-aspartate | HCID 2808532 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14626423 | HCID 14626423 | — |
Reaction Steps
The starting material was synthesised as follows. To a solution of hippuric acid (0.90 g, 5×10−3 moles) and L-aspartic acid dibenzyl ester (2.31 g, 5×10−3 moles) in DMF (35 ml) was added 1-hydroxybenzotriazole (0.73 g, 5.5×10−3 moles), triethylamine (1.4 ml, 9.7×10−3 moles) and 1-(3-dimethyl-aminopropyl)-3-ethylcarbodiimide, HCl salt (1.05 g, 5.5×10−3 moles). The mixture was stirred for 4 hours at room temperature then poured into water (450 ml) and extracted twice with ethyl acetate (100 ml). The extract was washed with saturated sodium bicarbonate solution, water, 2N HCl and water. The organic phase was dried over MgSO4 and evaporated to dryness to obtain the desired starting material as a yellow oil. 1.90 g (80%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06436691B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-0fd1f2ef19bd45af8c7c0c926aae33ca |
| Source note | uspto-grants-2002_08 |