HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-n-butyl-2,4-dihydro-2-[1-(N-methylcarbamoyl)ethyl]-4-[(2'-cyanobiphenyl-4-yl)methyl]-3H-1,2,4-triazol-3-one → HCID 178441927, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-n-butyl-2,4-dihydro-2-[1-(N-methylcarbamoyl)ethyl]-4-[(2'-cyanobiphenyl-4-yl)methyl]-3H-1,2,4-triazol-3-one | HCID 19939439 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178441927 | HCID 178441927 | 43% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
The conversion of 5-n-butyl-2,4-dihydro-2-[1-(N-methylcarbamoyl)ethyl]-4-[(2'-cyanobiphenyl-4-yl)methyl]-3H-1,2,4-triazol-3-one to the corresponding tetrazole was accomplished by the procedure of Example 9, Step E, except that the mixture was stirred at 120° C. for 2 days. After work-up, the residue was taken up in CH2Cl2 and flash chromatographed over silica gel (15 mL for 0.19 mmole, gradient elution using 5-30% MeOH/CH2Cl2 to give the desired compound as a white powder in 43% yield, homogeneous by TLC in 30% MeOH/CH2Cl2, mass spectrum (FAB) 461 (M+1)+, mp 153°-155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05411980 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-235f2d3ec61644bd9e14d82e7ad6db05 |
| Source note | uspto-grants-1995_05 |