HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 86736052, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl isocyanoacetate | HCID 533707 | — |
| Reactant | HCID 12441372 | HCID 12441372 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86736052 | HCID 86736052 | — |
Reaction Steps
Potassium t-butoxide, 1.4 g (0.0125 mole), was added to a solution of 1.4 g (0.0124 mole) of ethyl isocyanoacetate in 125 ml of dry tetrahydrofuran. After stirring under argon for 10 minutes, 5.07 g (0.01 mole) of 7-chloro-2-[bis(morpholino)-phosphinyloxy]-5-(2-fluorophenyl)-3H-1,4-benzodiazepine was added and stirring was continued for 30 minutes at room temperature. The reaction mixture was then acidified with glacial acetic acid, diluted with water and extracted with methylene chloride. The extracts were washed with saturated sodium bicarbonate solution, dried and evaporated. Crystallization of the residue from ether yielded crystals which were recrystallized from methylene chloride/ether/hexane for analysis, mp 195°-196°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04118386 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-25ac7fb488c44e43a7c3ee4728a4033d |
| Source note | uspto-grants-1978_10 |