HuagongsheHuagongshe Chemistry Print Report · For research reference only
18-Crown-6 → HCID 20562372, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 20562369 | HCID 20562369 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20562372 | HCID 20562372 | — |
Reaction Steps
3.7 g of 1-(2-chloroethyl)-3-[6-chloro-5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]urea dissolved in 100 ml of acetonitrile are treated with 1.83 g of potassium acetate and 4.21 g of 18-crown-6. The mixture is then stirred at room temperature for 5 days, concentrated, treated with water/methylene chloride and the aqueous solution is extracted several times with methylene chloride. The organic solution is dried with sodium sulphate, filtered and concentrated. The residue is purified on a 350 g silica gel column using ethyl acetate as the eluting agent and crystallised from ethanol/ether. There is obtained 2-[3-[6-chloro-5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]ureido]ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04294758 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-afb0ad81616e453ca6e60b58c358b12b |
| Source note | uspto-grants-1981_10 |