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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043765Generated: October 26, 2026

Dichloromethane → 2-Amino-5-bromo-4-methoxypyrimidine

https://huagongshe.com/reaction/1043765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Methoxy-2-pyrimidinamineHCID 67428—
SolventChloroformHCID 6212—
Product2-Amino-5-bromo-4-methoxypyrimidineHCID 4503693796%

Reaction Steps

To a solution of 4-methoxypyrimidine-2-ylamine (1.84 g, 14.7 mmol) in chloroform (600 mL) was added N-bromosuccinimide (2.62 g, 14.7 mmol). After stirring in the dark for 5 hours, the solution was added to CH2Cl2 (200 mL) and 1N NaOH (100 mL). Upon mixing, the layers were separated and the organic layer was washed with NaCl(sat.) (100 mL), dried over Na2SO4, filtered and concentrated yielding 2.88 g (96%) of 5-bromo-4-methoxypyrimidine-2-ylamine. LCMS (m/z): 204/206 (MH+). 1H NMR NMR (CDCl3): δ 8.10 (s, 1H), 4.93 (bs, 2H), 3.96 (s, 31-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563549B2
Source datasetuspto-grants-2013_10
ORD IDord-a145154cd71d414a8031322f61d46659
Source noteuspto-grants-2013_10