HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67255662, compound → HCID 67254134, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67255662 | HCID 67255662 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67254134 | HCID 67254134 | — |
Reaction Steps
A solution of the crude 3-(2-tert-Butoxycarbonylamino-4-methyl-phenoxymethyl)-3,4-dihydro-2H-quinoline-1-carboxylic acid benzyl ester (crude, 0.35 mmol) in 4N HCl in dioxane (2 mL) at room temperature was stirred under a drying tube overnight. The suspension was concentrated by rotovap, diluted to 30 mL with CH2Cl2 and shaken with 10% Na2CO3 (30 mL). The organics were isolated, dried (MgSO4), filtered and concentrated to a brown oil corresponding to the crude aniline, which was used without purification in the urea forming reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067506B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-912bedee837640a7b13917a5db25fba1 |
| Source note | uspto-grants-2006_06 |