Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726297Generated: October 26, 2026

6-Bromopyridin-3-amine → Tert-butyl 4-((6-bromopyridin-3-yl)amino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1726297

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromopyridin-3-amineHCID 642811—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ProductTert-butyl 4-((6-bromopyridin-3-yl)amino)piperidine-1-carboxylateHCID 8660214058%

Reaction Steps

Using general procedure A, 5-amino-2-bromopyridine (Binz; v, Schickh, Chem. Ber., 68, 1935, 315-321) (308 mg, 1.78 mmol) and 1-Boc-4-piperidone (317 mg, 1.59 mmol) gave 4-(6-bromo-pyridin-3-ylamino)-piperidine-1-carboxylic acid tert-butyl ester as a yellow solid (326 mg, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-bb1d3ce785e44ec4bf9c31dd038b667e
Source noteuspto-grants-2009_02