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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446611Generated: October 27, 2026

3-(Methylamino)propanoic acid, N-BOC protected → Benzyl {6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}(4-{[N-(tert-butoxycarbonyl)-N-methyl-beta-alanyl](methyl)amino}phenyl)carbamate

https://huagongshe.com/reaction/446611

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylamino)propanoic acid, N-BOC protectedHCID 2760952—
ReactantBenzyl {6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}[4-(methylamino)phenyl]carbamateHCID 66671650—
ProductBenzyl {6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}(4-{[N-(tert-butoxycarbonyl)-N-methyl-beta-alanyl](methyl)amino}phenyl)carbamateHCID 66793891112.2%

Reaction Steps

N-(tert-Butoxycarbonyl)-N-methyl-β-alanine (41 mg, 0.19 mmol) and the compound (150 mg, 0.21 mmol) obtained in Example 97c were used to give the title compound (190 mg; yield, 100%) 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-12c2398d6613446e8a7cfb7e548cb84f
Source noteuspto-grants-2013_07