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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264613Generated: October 28, 2026

Sodium borohydride → (2R*,4S*)-2-benzyl-1-(3-trifluoromethylbenzoyl)-N-(4-quinolylmethyl)-4-piperidinamine

https://huagongshe.com/reaction/264613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(2R*,4S*)-2-Benzyl-1-(3-trifluoromethylbenzoyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamineHCID 57043812—
Product(2R*,4S*)-2-benzyl-1-(3-trifluoromethylbenzoyl)-N-(4-quinolylmethyl)-4-piperidinamineHCID 57086513—

Reaction Steps

0.184 g (0.307 mmol) of (2R*,4S*)-2-benzyl-1-(3-trifluoromethylbenzoyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine is reacted with 0.046 g (1.23 mmol) of sodium borohydride in analogy to Example 2. The title compound of the formula ##STR29## is obtained as yellow oil. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.28, FD-MS: M+ =503.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646144
Source datasetuspto-grants-1997_07
ORD IDord-48c552fd791a4cddb05716dd6d3e0f51
Source noteuspto-grants-1997_07