HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 19081190, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86752747 | HCID 86752747 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19081190 | HCID 19081190 | — |
Reaction Steps
A mixture of N-[(3RS)-1-(3-azabicyclo[3.2.2]non-3-yl)-carbonylmethyl-2,3-dihydro-5-(2-fluorophenyl)-2-oxo-1H-1,4-benzodiazepin-3-yl]-N'-[3-(ethoxycarbonylmethoxy)phenyl]urea and 0.1N NaOH in tetrahydrofuran was stirred at room temperature for 6 hours. 1N HCl was added to the reaction mixture. Ethyl acetate and water were added to the reaction mixture, and the organic layer was removed, washed with water and brine, and dried over magnesium sulfate. The solution was evaporated to dryness and washed with isopropyl ether and diethyl ether to afford N-[(3RS)-1-(3-azabicyclo[3.2.2]non-3-yl)carbonylmethyl-2,3-dihydro-5-(2-fluorophenyl)-2-oxo-1H-1,4-benzodiazepin-3-yl]-N'-(3-carboxymethoxyphenyl)urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763437 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-8ae6210201164fbf9df4c613edc3b6fe |
| Source note | uspto-grants-1998_06 |