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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446536Generated: October 29, 2026

tert-Butyl 4-(methylamino)benzoate → tert-Butyl-4-[{7-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-7-oxoheptyl}(methyl)amino]benzoate

https://huagongshe.com/reaction/446536

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(methylamino)benzoateHCID 22291264—
Reactant1-{2-[(7-Hydroxyheptanoyl)(methyl)amino]ethyl}piperidin-4-yl biphenyl-2-ylcarbamateHCID 66671691—
Producttert-Butyl-4-[{7-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-7-oxoheptyl}(methyl)amino]benzoateHCID 6679379826%

Reaction Steps

The compound (163 mg, 0.338 mmol) obtained in Example 39b was used according to the method described in Example 4g to give a crude aldehyde compound (160 mg). The resulting crude aldehyde compound and the compound (69 mg, 0.334 mmol) obtained in Example 35a were used a to give the title compound (58 mg; yield, 26%) as a white solid according to the method described in Example 18b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476253B2
Source datasetuspto-grants-2013_07
ORD IDord-b9877a9894fa46bf9c25d28370f9c3f3
Source noteuspto-grants-2013_07