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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251142Generated: November 1, 2026

4-Amino-1-Boc-piperidine → 4-[(3-Phenyl-pyridin-2-ylmethyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/251142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Phenyl-2-pyridinecarboxaldehydeHCID 10773808—
Product4-[(3-Phenyl-pyridin-2-ylmethyl)-amino]-piperidine-1-carboxylic acid tert-butyl esterHCID 67273605—

Reaction Steps

Under General Procedure B: Reaction of 3-phenyl-pyridine-2-carbaldehyde and 4-amino-piperidine-1-carboxylic acid tert-butyl ester (Huang, Y. et al. J. Med. Chem. 2001, 44, 4404-4415) in MeO4 with NaBH4 gave 4-[(3-phenyl-pyridin-2-ylmethyl)-amino]-piperidine-1-carboxylic acid tert-butyl ester. 1H NMR (CDCl3) δ 1.22 (m, 3H), 1.41 (s, 9H), 1.70 (m, 2H), 2.52 (m, 1H), 2.72 (m, 3H), 3.84 (s, 2H), 7.21 (q, 1H, J=4.03 Hz), 7.32 (m, 2H), 7.40 (m, 3H), 7.53 (dd, 1H, J=7.79, 1.72 Hz), 8.54 (m, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863293B2
Source datasetuspto-grants-2011_01
ORD IDord-0b6b4eb719db4406addcb7b97d12b116
Source noteuspto-grants-2011_01