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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033310Generated: November 2, 2026

Sodium borohydride → HCID 57256727, compound

https://huagongshe.com/reaction/1033310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57028147HCID 57028147—
ProductHCID 57256727HCID 57256727—

Reaction Steps

128 mg (0.225 mmol) of (2R*,4S*)-2-benzyl-1-(4-quinolylmethyl) N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine are reacted with 34 mg (0.872 mmol) of sodium borohydride in analogy to Example 2. The title compound ##STR39## is obtained as yellow oil. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.45, FD-MS: M+ =490.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310743
Source datasetuspto-grants-1994_05
ORD IDord-0685bd1be35b44b99ba69c9cc8e4f346
Source noteuspto-grants-1994_05