HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 57308337, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 57305705 | HCID 57305705 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 57308337 | HCID 57308337 | — |
Reaction Steps
To a solution of 17-ethyl-20-fluoro-1, 14-dihydroxy-12-[2'-(3"-methoxy-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 from Example 24 (79.7 mg) in dry isopropyl alcohol (3 ml) is added benzylamine (86.5 mg). The mixture is stirred at r.t. for 30 min., 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 | US05189042 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-161a5a44773d45bbaad0d503e22ec46b |
| Source note | uspto-grants-1993_02 |