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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772885Generated: November 1, 2026

Di-tert-butyl dicarbonate → Tert-butyl(6-bromo-3-methoxypyridin-2-yl)carbamate

https://huagongshe.com/reaction/1772885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant2-Amino-6-bromo-3-methoxypyridineHCID 57562906—
ReactantDi-tert-butyl(6-bromo-3-methoxypyridin-2-yl)imidodicarbonateHCID 118685198—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductTert-butyl(6-bromo-3-methoxypyridin-2-yl)carbamateHCID 131734688—

Reaction Steps

A mixture of 6-bromo-3-methoxypyridin-2-amine (10.2 g, 50.2 mmol), Boc2O (38.2 g, 0.18 mol) and 4-(dimethylamino)pyridine (1.2 g, 9.82 mmol) in MeCN (550 mL) was refluxed for 2 h. After cooling to rt and concentration in vacuo EtOAc (500 mL) was added and the organic phase washed with water (100 mL) and brine (50 mL). The organic phase was dried (MgSO4), filtered and the filtrate concentrated in vacuo. Purification by chromatography eluting with 4:1 DCM-heptane yielded a mixture of the title compound and di-tert-butyl(6-bromo-3-methoxypyridin-2-yl)imidodicarbonate (10.6 g) in an approximate ratio of 55:45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249160B2
Source datasetuspto-grants-2016_02
ORD IDord-0c5f5d9864ed461fa7bcf07e8b4192b3
Source noteuspto-grants-2016_02