HuagongsheHuagongshe Chemistry Print Report · For research reference only
n-Heptyl isocyanate → Methyl 3-[3'-(3-heptyl-1-methylureido)-2-methoxybiphenyl-4-yl]propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | n-Heptyl isocyanate | HCID 138341 | — |
| Reactant | Methyl 3-(2-methoxy-3'-methylaminobiphenyl-4-yl)propanoate | HCID 67273007 | — |
| Reactant | Triethylamine tetrahydrofuran | HCID 68616177 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-[3'-(3-heptyl-1-methylureido)-2-methoxybiphenyl-4-yl]propanoate | HCID 67272737 | 72.2% |
Reaction Steps
540 μL (3.3 mmol, 2 eq) of heptyl isocyanate are added to a solution of 495 mg (1.65 mmol, 1 eq) of methyl 3-(2-methoxy-3′-methylaminobiphenyl-4-yl)propanoate in 10 mL of an 8/2 tetrahydrofuran/triethylamine mixture. The reaction mixture is stirred for 12 hours at room temperature. The reaction medium is hydrolyzed in water and then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (70/30 heptane/ethyl acetate). 525 mg of methyl 3-[3′-(3-heptyl-1-methylureido)-2-methoxybiphenyl-4-yl]propanoate are obtained in oil form. Yield=72%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863332B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-cc0a2df2975d4b1cbb3a22253289dd34 |
| Source note | uspto-grants-2011_01 |