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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033357Generated: October 26, 2026

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

https://huagongshe.com/reaction/1033357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIndole-2-carboxylic acidHCID 72899—
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-(2-indolylcarbonyl)-4-piperidinamineHCID 57278312—

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 106 mg (0.661 mmol) of indole-2-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 ##STR87## is obtained (89 mg, 32%) as white crystals with melting point 254° C. TLC: methylene chloride/methanol/conc. ammonia (2000:50:1) Rf =0.56, FD-MS: M+ =505, 507; IR: 3430, 3290, 1625 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310743
Source datasetuspto-grants-1994_05
ORD IDord-f5807c40951d4d3392ef233ab4cff71e
Source noteuspto-grants-1994_05