HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-benzyl-3-[(E)-[1-[2-[di(propan-2-yl)amino]ethyl]-2-oxoindol-3-ylidene]amino]urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Benzylsemicarbazide hydrochloride | HCID 12401712 | — |
| Reactant | 1-(2-Diisopropylaminoethyl)isatin | HCID 13934408 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-benzyl-3-[(E)-[1-[2-[di(propan-2-yl)amino]ethyl]-2-oxoindol-3-ylidene]amino]urea | HCID 178457397 | 57.5% |
Reaction Steps
To a suspension of 1.37 g of 1-(2-diisopropylaminoethyl)isatin and 1.20 g of 4-benzylsemicarbazide hydrochloride in 20 ml of a mixture of ethanol and water (2:1) was added 0.50 g of sodium acetate. The mixture was stirred for 18 hours at room temperature, and then concentrated under reduced pressure. An aqueous sodium bicarbonate solution was added to the residue. The precipitates were collected by filtration, washed with water, and recrystallized from aqueous ethanol to obtain 1.21 g of (E)-1-(2-diisopropylaminoethyl)isatin 3-(4-benzylsemicarbazone) having a melting point of 164°-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04780477 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-65eb94696a494d4da8d110106b4ca69d |
| Source note | uspto-grants-1988_10 |