HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 57094336, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57130757 | HCID 57130757 | — |
| Product | HCID 57094336 | HCID 57094336 | — |
Reaction Steps
128 mg (0.218 mmol) of (2R *,4S*)-2-benzyl-1-(2,4-dichlorobenzyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine are reacted with 34 mg (0.920 mmol) of sodium borohydride in analogy to Example 2. The title compound ##STR40## is obtained as yellow oil. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.25, FD-MS: M+ =472.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646144 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-5849fade6e474f1e832588bd5a537322 |
| Source note | uspto-grants-1997_07 |