HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-[2-(4-Cyanophenyl)ethyl]quinazolin-7-yl-carboxylic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-Phenyl-beta-alanine methyl ester | HCID 89103 | — |
| Reactant | 2-[2-(4-Cyanophenyl)-ethyl]-quinazoline-7-carboxylic acid | HCID 18412447 | — |
| Product | 2-[2-(4-Cyanophenyl)ethyl]quinazolin-7-yl-carboxylic acid-n-phenyl-n-(2-methoxycarbonylethyl)amide | HCID 18412551 | — |
Reaction Steps
0.4 g (1.3 mmol) of 2-[2-(4-cyanophenyl)-ethyl]-quinazoline-7-carboxylic acid and 5 ml of thionyl chloride were stirred for 60 minutes at 50° C. Then the thionyl chloride was distilled off, the residue was dissolved in methylene chloride, mixed with 0.24 g (1.3 mmol) of methyl 3-(N-phenylamino)-propionate and 0.22 ml of (1.3 mmol) of N-ethyldiisopropylamine and stirred for 18 hours at ambient temperature. After evaporation of the solvent in vacuo the residue was chromatographed on silica gel and eluted with methylene chloride containing 1% methanol. Yield: 230 mg (37% of theory), Rf value: 0.64 (silica gel, methylene chloride/methanol=9:1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06087380 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-8a402f14eed44a6d9ffda1c29da29114 |
| Source note | uspto-grants-2000_07 |