Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737053Generated: October 27, 2026

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

https://huagongshe.com/reaction/1737053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIndole-3-Carboxylic AcidHCID 69867—
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-(3-indolylcarbonyl)-4-piperidinamineHCID 57038839—

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-3-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 ##STR86## is obtained (92 mg, 33%) as oil. TLC: methylene chloride/methanol/conc. ammonia (350:50:1) Rf =0.61, FD-MS: M+ =505,507; IR: 3450, 3260, 1770, 1635 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541195
Source datasetuspto-grants-1996_07
ORD IDord-5681875a6e8449958261311b02660f46
Source noteuspto-grants-1996_07