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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264629Generated: October 31, 2026

Sodium borohydride → (2R*,4S*)-2-benzyl-1-(2-naphthylacetyl)-N-(4-quinolylmethyl)-4-piperidinamine

https://huagongshe.com/reaction/264629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(2R*,4S*)-2-benzyl-1-(2-naphthylacetyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamineHCID 57233831—
Product(2R*,4S*)-2-benzyl-1-(2-naphthylacetyl)-N-(4-quinolylmethyl)-4-piperidinamineHCID 57015386—

Reaction Steps

160 mg (0.269 mmol) of (2R*,4S*)-2-benzyl-1-(2-naphthylacetyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine are reacted with 42 mg (1.13 mmol) of sodium borohydride in analogy to Example 2. The title compound ##STR38## is obtained as colourless oil. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.27, FD-MS: M+ =499.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646144
Source datasetuspto-grants-1997_07
ORD IDord-988691b72b57497e982304ccfa944223
Source noteuspto-grants-1997_07