HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 57232360, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57325230 | HCID 57325230 | — |
| Product | HCID 57232360 | HCID 57232360 | — |
Reaction Steps
80 mg (0.142 mmol) of (2R*,4S*)-2-benzyl-1-(benzyloxycarbonyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine are reacted with 22 mg (0.57 mmol) of sodium borohydride in analogy to Example 2. The title compound ##STR36## is obtained as colourless oil. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.43, FD-MS: M+ =465.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541195 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-b1d30b59836b4ea3b2f2cee9162ba2e3 |
| Source note | uspto-grants-1996_07 |