HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052505Generated: November 2, 2026
Benzyloxycarbonylglycine → HCID 131736174, compound
https://huagongshe.com/reaction/1052505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyloxycarbonylglycine | HCID 14349 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | HCID 70979311 | HCID 70979311 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131736174 | HCID 131736174 | 92.1% |
Reaction Steps
DIEA (10.5 ml, 60 mmol) was added at 0° C. over a mixture of 1-amino-3-bromo-N-phenyl-1H-pyrrole-2-carboxamide (5.1 g, 18 mmol) and 2-(benzyloxycabonylamino)acetic acid (5.33 g, 25 mmol) in anhydrous ethyl acetate (100 ml). After 15 min T3P® solution (50% AcOEt, 15 ml) was slowly added and stirred 20 min at 0° C. and then at room temperature overnight. Further DIEA (5 ml, 30 mmol), 2-(benzyloxycabonylamino)acetic acid (2.66 g, 25 mmol) and T3P® solution (50% AcOEt, 7 ml) were added and the reaction mixture was stirred at room temperature overnight. More ethyl acetate was added and the reaction crude was washed with water and brine, dried over magnesium sulphate and the solvent was removed under vacuum. The residue was purified by flash chromatography using Isolera® Purification System (0-40%, hexane-AcOEt) to give 7.81 g (41% yield) of the final product with a purity of 45% that was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09388189B2 |
|---|
| Source dataset | uspto-grants-2016_07 |
|---|
| ORD ID | ord-29a4e3914499492096d83fc6ec8fa133 |
|---|
| Source note | uspto-grants-2016_07 |
|---|