HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-Formyl-[1,1'-biphenyl]-2-carbonitrile → HCID 22852213, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-Formyl-[1,1'-biphenyl]-2-carbonitrile | HCID 1394062 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Isoleucine methyl ester hydrochloride | HCID 11171351 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 22852213 | HCID 22852213 | — |
Reaction Steps
The starting material can be obtained, for example, analogously to Example 1b): The reaction of 2.0 g of 2'-cyanobiphenyl-4-carbaldehyde, 9.6 g of molecular sieve 5 A, 1.76 g of (L)-isoleucine methyl ester hydrochloride and 680 mg of sodium cyanoborohydride yields N-[(2'-cyanobiphenyl-4-yl)methyl]-(L)-isoleucine methyl ester after flash chromatography (ethyl acetate/hexane 1:3). 1H-NMR (DMSO): 1.21 ppm (d, 3H), 3.63 ppm (s, 3H), 3.75 (dd, 1H), 4.56 ppm (d, 2H), 4.58 ppm (d, 2H), 5.31 ppm (t, 1H), 7.4-8 ppm aromatics.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05399578 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-892c6d934b85430a9f3f6de493a9418f |
| Source note | uspto-grants-1995_03 |