HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 57127501, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 57263521 | HCID 57263521 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 57127501 | HCID 57127501 | — |
Reaction Steps
To a solution of 17-ethyl-1,14-dihydroxy-12-[2'-(3"-phenoxy-4"-oxocyclohexyl]-1'-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone in dry isopropyl alcohol (3 ml) is added benzyl amine (87 mg). The mixture is stirred at r.t. for 30 minutes, and cooled to -78° C. To this solution is added a solution of sodium cyanoborohydride (6.7 mg) in isopropyl alcohol (0.5 ml). The reaction is stirred at -78° C. and poured into ice water. Extraction with ethyl acetate, followed by purification gives the title compound as a mixture of epimers at C-4".
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05262533 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-feb92199b05548dcb58d05dfbd5d6479 |
| Source note | uspto-grants-1993_11 |