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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736982Generated: October 31, 2026

Sodium borohydride → HCID 57232360, compound

https://huagongshe.com/reaction/1736982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57325230HCID 57325230—
ProductHCID 57232360HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541195
Source datasetuspto-grants-1996_07
ORD IDord-b1d30b59836b4ea3b2f2cee9162ba2e3
Source noteuspto-grants-1996_07