HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 178463452, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Boc-arg(boc)2-OH | HCID 11385959 | — |
| Reactant | methyl ((3R,4R)-1-(2-chloro-5-cyano-3-((7-cyano-4-(ethylamino)imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)-3-hydroxypiperidin-4-yl)carbamate | HCID 89932121 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178463452 | HCID 178463452 | — |
Reaction Steps
To a solution of (Example 328) methyl ((3R,4R)-1-(2-chloro-5-cyano-3-((7-cyano-4-(ethylamino)imidazo[2,1-f][1,2,4]triazin-2-yl)amino)phenyl)-3-hydroxypiperidin-4-yl)carbamate (50 mg, 0.098 mmol), BOC-ARG(BOC)2-OH (96 mg, 0.202 mmol), DMAP (2.391 mg, 0.020 mmol) and DCC (60.6 mg, 0.294 mmol) were dissolved in DCM (5 mL) under nitrogen. The reaction mixture was stirred at room temperature 12 hr; the LCMS showed complete conversion. The solvent was removed and the material was diluted with acetone and filtered (removes 1,3-dicyclohexylurea).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273057B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-9e9b0693768f44a1955d1165e067d9f7 |
| Source note | uspto-grants-2016_03 |