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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737052Generated: October 26, 2026

Triethylamine → (2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-(4-quinolylcarbonyl)-4-piperidinamine

https://huagongshe.com/reaction/1737052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Quinolinecarboxylic acidHCID 10243—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
Reactant(2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamineHCID 53839030—
Product(2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-N-(4-quinolylcarbonyl)-4-piperidinamineHCID 44288896—

Reaction Steps

200 mg (0.550 mmol) of (2R*,4S*)-2-benzyl-1-(3,5-dichlorobenzoyl)-4-piperidinamine are reacted in analogy to Example 4a with 105 mg (0.660 mmol) of quinoline-4-carboxylic acid, 168 mg (0.661 mmol) of bis(2-oxo-3-oxazolidinyl)phosphinic chloride and 169 μl (1.21 mmol) of triethylamine. The title compound ##STR85## is obtained (278 mg, 97%) as oil. TLC: methylene chloride/methanol/conc. ammonia (700:50:1) Rf =0.45, FD-MS: M+ =517, 519; IR: 3395, 1755, 1620 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541195
Source datasetuspto-grants-1996_07
ORD IDord-af4441405c3742ab81d5025214f9a9bc
Source noteuspto-grants-1996_07