HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Tert-butyl 1-(4-chlorophenyl)-3-ureidopropylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-butyl N-[1-(4-chlorophenyl)-3-(phenoxycarbonylamino)propyl]carbamate | HCID 57750354 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 1-(4-chlorophenyl)-3-ureidopropylcarbamate | HCID 57750307 | 100.5% |
Reaction Steps
Ammonium chloride (113 mg, 2.11 mmol) was added in one portion to tert-butyl N-[1-(4-chlorophenyl)-3-(phenoxycarbonylamino)propyl]carbamate (Intermediate 109) (427 mg, 1.05 mmol) and triethylamine (0.882 mL, 6.33 mmol) in DMF (3 mL). The resulting solution was stirred at 0.352 molar for 24 hours. The reaction mixture was concentrated and diluted with EtOAc (20 mL) and washed with water (20 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford tert-butyl 1-(4-chlorophenyl)-3-ureidopropylcarbamate (346 mg, 100%),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101623B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-1dbc59e56a43492c9c74bc2a6ce38c88 |
| Source note | uspto-grants-2012_01 |