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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446544Generated: October 27, 2026

4-[2-(N-Boc-N-methylamino)ethyl]benzoic acid → tert-Butyl (2-{4-[{3-[({[(2S)-1'-{2-[(5R)-3-[3,5-bis(trifluoromethyl)benzoyl]-5-(4-fluorophenyl)-1,3-oxazolidin-5-yl]ethyl}-2,3-dihydrospiro[indene-1,4'-piperidin]-2-yl]oxy}acetyl)(methyl)amino]propyl}(methyl)carbamoyl]phenyl}ethyl)methylcarbamate

https://huagongshe.com/reaction/446544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[2-(N-Boc-N-methylamino)ethyl]benzoic acidHCID 66671362—
Reactant2-{[(2S)-1'-{2-[(5R)-3-[3,5-Bis(trifluoromethyl)benzoyl]-5-(4-fluorophenyl)-1,3-oxazolidin-5-yl]ethyl}-2,3-dihydrospiro[indene-1,4'-piperidin]-2-yl]oxy}-N-methyl-N-[3-(methylamino)propyl]acetamideHCID 86663419—
Producttert-Butyl (2-{4-[{3-[({[(2S)-1'-{2-[(5R)-3-[3,5-bis(trifluoromethyl)benzoyl]-5-(4-fluorophenyl)-1,3-oxazolidin-5-yl]ethyl}-2,3-dihydrospiro[indene-1,4'-piperidin]-2-yl]oxy}acetyl)(methyl)amino]propyl}(methyl)carbamoyl]phenyl}ethyl)methylcarbamateHCID 8666344892%

Reaction Steps

The compound (140 mg, 0.501 mmol) obtained in Example 50a and the compound (260 mg, 334 mol) obtained in Example 1k were used to give the title compound (320 mg; yield, 92%) as a white solid according to the method described in Example 41a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476253B2
Source datasetuspto-grants-2013_07
ORD IDord-bbcea42410404bcd815290b0d54aadce
Source noteuspto-grants-2013_07