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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158949Generated: October 27, 2026

4-Amino-4'-cyanobiphenyl → 6-({3-Benzyloxy-5-[(4'-cyano-biphenyl-4-ylamino)-methyl]-2-methyl-pyridin-4-ylmethyl}-tert-butoxycarbonyl-amino)-hexanoic acid benzyl ester

https://huagongshe.com/reaction/1158949

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-4'-cyanobiphenylHCID 97193—
Reactant6-[(3-Benzyloxy-5-formyl-2-methyl-pyridin-4-ylmethyl)-tert-butoxycarbonyl-amino]-hexanoic acid benzyl esterHCID 58636791—
Product6-({3-Benzyloxy-5-[(4'-cyano-biphenyl-4-ylamino)-methyl]-2-methyl-pyridin-4-ylmethyl}-tert-butoxycarbonyl-amino)-hexanoic acid benzyl esterHCID 5863671583.3%

Reaction Steps

The reductive amination of 6-[(3-benzyloxy-5-formyl-2-methyl-pyridin-4-ylmethyl)-tert-butoxycarbonyl-amino]-hexanoic acid benzyl ester (2.2 g, 3.9 mmol) and 4-amino-4′-cyanobiphenyl (2.1 g, 10.8 mmol), as described in Example 21, gave 6-({3-benzyloxy-5-[(4′-cyano-biphenyl-4-ylamino)-methyl]-2-methyl-pyridin-4-ylmethyl}-tert-butoxycarbonyl-amino)-hexanoic acid benzyl ester (44) (2.4 g, 83% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812037B2
Source datasetuspto-grants-2010_10
ORD IDord-b2440f1bf1cf4ce1998f144d8ec4f4c5
Source noteuspto-grants-2010_10