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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043764Generated: October 30, 2026

2-Pyrimidinamine, 4-chloro-6-methoxy- → 4-Methoxy-2-pyrimidinamine

https://huagongshe.com/reaction/1043764

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyrimidinamine, 4-chloro-6-methoxy-HCID 79811—
ReactantDiisopropylethylamineHCID 81531—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product4-Methoxy-2-pyrimidinamineHCID 6742890%

Reaction Steps

To a solution of 4-chloro-6-methoxypyrimidine-2-ylamine (4.4 g, 27.7 mmol) in EtOAc (200 mL) and ethanol (150 mL), was added diisopropylethylamine (9.6 mL, 55.3 mmol) and 10% palladium on carbon (2.9 g, 2.77 mmol). The heterogeneous solution was stirred under a balloon atmosphere of H2 for 14 hours, at which time the solution was filtered through a Celite pad and the volatiles were removed in vacuo. The residue was dissolved in EtOAc (200 mL), washed with Na2CO3(sat.) (100 mL) and with NaCl(sat.) (100 mL), dried over Na2SO4, filtered and concentrated yielding 3.1 g (90%) of 4-methoxypyrimidine-2-ylamine. LCMS (m/z): 126 (MH+). 1H NMR. (CDCl3): δ 8.00 (d, J=5.7 Hz, 1H), 6.08 (d, J=5.7 Hz, 1H), 4.98 (bs, 2H), 3.84 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563549B2
Source datasetuspto-grants-2013_10
ORD IDord-f02aa13e29534ec0a5b63d155cebc2ca
Source noteuspto-grants-2013_10