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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18254Generated: October 25, 2026

Bromine → Methyl 2-amino-5-bromonicotinate

https://huagongshe.com/reaction/18254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantMethyl 2-aminopyridine-3-carboxylateHCID 351633—
SolventAcetic AcidHCID 176—
ProductMethyl 2-amino-5-bromonicotinateHCID 276345398.2%

Reaction Steps

Bromine (0.7 mL, 14 mmole) was added dropwise to a stirred solution of methyl 2-aminonicotinate (2.0 g, 13 mmole) in HOAc (50 mL). A suspension formed within 30 min. The reaction was allowed to stir at room temperature for 2 h, then was concentrated under vacuum. The residue was triturated with 1.0 N Na2CO3 (50 mL) and the solid was collected by suction filtration. The solid was washed with H2O (50 mL) and dried under vacuum to give the title compound (2.95 g, 98%) as a pale yellow solid: 1H NMR (400 MHz, CDCl3) δ 8.24 (d, J=2.5 Hz, 1 H), 8.23 (d, J=2.5 Hz, 1 H), 6.40 (br s, 2 H), 3.90 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741339B2
Source datasetuspto-grants-2010_06
ORD IDord-6b785971e87942358a742a706360fd1c
Source noteuspto-grants-2010_06