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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011501Generated: October 31, 2026

2-Amino-5-bromopyridine → 2-(Boc-amino)-5-bromopyridine

https://huagongshe.com/reaction/1011501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
Product2-(Boc-amino)-5-bromopyridineHCID 16217843—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-amino-5-bromopyridine (8.65 g, 50 mmol) in THF (100 mL) was added lithium hexamethyldisilazide (105 mL, 105 mmol) under nitrogen at 0° C. After the addition, the mixture was stirred for 30 mins at 0° C. At this point, (BOC)2O (12 g, 55 mmol) was added to the reaction mixture and the mixture was stirred for another 30 mins at 0° C. TLC (petroleum ether/ethyl acetate=5:1) indicated the reaction was complete. The reaction mixture was washed with 1 N HCl (20 mL), and the residue was extracted with ethyl acetate (50 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, and evaporated in vacuo. The residue was purified by chromatography on silica to afford (I-29a) (8 g, 58.6%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977367B2
Source datasetuspto-grants-2011_07
ORD IDord-839116770acb4b3ba3ae0f9d8376e73a
Source noteuspto-grants-2011_07