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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264632Generated: October 31, 2026

Sodium borohydride → HCID 57094336, compound

https://huagongshe.com/reaction/264632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57130757HCID 57130757—
ProductHCID 57094336HCID 57094336—

Reaction Steps

128 mg (0.218 mmol) of (2R *,4S*)-2-benzyl-1-(2,4-dichlorobenzyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine are reacted with 34 mg (0.920 mmol) of sodium borohydride in analogy to Example 2. The title compound ##STR40## is obtained as yellow oil. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.25, FD-MS: M+ =472.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646144
Source datasetuspto-grants-1997_07
ORD IDord-5849fade6e474f1e832588bd5a537322
Source noteuspto-grants-1997_07