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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262185Generated: October 26, 2026

tert-Butyl 4-(5-aminopyridin-2-yl)piperidine-1-carboxylate → (1',2',3',4',5',6'-Hexahydro-[2,4]bipyridinyl-5-yl)-[7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-amine

https://huagongshe.com/reaction/1262185

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(5-aminopyridin-2-yl)piperidine-1-carboxylateHCID 59128562—
Reactant7-(2-Methoxyphenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-olHCID 178489276—
Product(1',2',3',4',5',6'-Hexahydro-[2,4]bipyridinyl-5-yl)-[7-(2-methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-amineHCID 46851866—

Reaction Steps

This example was prepared by using 5-Amino-3′,4′,5′,6′-tetrahydro-2′H-[2,4]bipyridinyl-1′-carboxylic acid tert-butyl ester (WO2006/047277) and 7-(2-Methoxy-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-ol as described in Example 1255c followed by deprotection as described in Example 1223. 1H-NMR (DMSO) δ 9.7 (s, 1H), 9.0 (s, 1H), 8.8 (s, 1H), 8.6 (m, 1H), 8.3 (m, 1H), 8.1 (d, J=8.5 Hz, 1H), 7.7 (d, J=7.5 Hz, 1H), 7.5 (t, 1H), 7.2 (m, 2H), 7.1 (t, 1H), 7.0 (m, 2H), 3.8 (s, 3H), 3.4 (m, 2H), 3.0 (m, 3H), 2.0 (m, 2H), 1.85 (m, 2H); LC/MS (ESI+): 401 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-6c8e80a0213d4459883bcfcd35e5799b
Source noteuspto-grants-2013_06