HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Tert-butyl 1-(4-(3-phenylureido)phenylsulfonyl)-1,2,3,4-tetrahydroquinolin-3-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tert-butyl 1-(4-aminophenylsulfonyl)1,2,3,4-tetrahydroquinolin-3-ylcarbamate | HCID 59400239 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Tert-butyl 1-(4-(3-phenylureido)phenylsulfonyl)-1,2,3,4-tetrahydroquinolin-3-ylcarbamate | HCID 59400148 | — |
Reaction Steps
tert-butyl 1-(4-aminophenylsulfonyl)-1,2,3,4-tetrahydroquinolin-3-ylcarbamate (60.5 mg, 0.15 mmol) and isocyantobenzene (17.8 mg, 0.15 mmol) in 1,2-dichloroethane (3 mL) were stirred at room temperature for 20 hours. Water (1.5 mL) was added and the mixture extracted with ethyl acetate (3×1.5 mL). The combined organics were dried over sodium sulfate and concentrated to give tert-butyl 1-(4-(3-phenylureido)phenylsulfonyl)-1,2,3,4-tetrahydroquinolin-3-ylcarbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273754B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-46e74c914f8a43c5afacc01998c38fb7 |
| Source note | uspto-grants-2012_09 |