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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420519Generated: October 30, 2026

N-bromobutanimide → Methyl 2-amino-5-bromoisonicotinate

https://huagongshe.com/reaction/420519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-aminopyridine-4-carboxylateHCID 236984—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-amino-5-bromoisonicotinateHCID 2530723035.4%

Reaction Conditions

Temperature-18 °C

Reaction Steps

A solution of 2-amino-isonicotinic acid methyl ester (5.58 g, 36.7 mmol) in DMF (56 mL) was cooled to −18° C. (ice/MeOH bath), treated with NBS (7.21 g, 38.5 mmol), and stirred at −18° C. for 1 h. The reaction mixture was diluted in AcOEt (500 mL) and washed with water (2×250 mL). The organic layer was dried over Na2SO4, filtered and evaporated to yield the crude title compound (3.0 g, 13.0 mmol, 35%) as a yellow solid, which was used in the next step without further purification. MS: 231 [M+1]+; HPLC: AtRet=0.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097617B2
Source datasetuspto-grants-2012_01
ORD IDord-e9ee3d3716b4441ea531b3b4e400860c
Source noteuspto-grants-2012_01