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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517459Generated: November 4, 2026

2-Methoxyethanol → 6-Chloro-4-(2-methoxyethoxy)pyrido[3,2-d]pyrimidin-2-amine

https://huagongshe.com/reaction/1517459

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant6-Chloro-4-(1H-1,2,4-triazol-1-yl)pyrido[3,2-d]pyrimidin-2-amineHCID 57698314—
SolventDichloromethaneHCID 6344—
Product6-Chloro-4-(2-methoxyethoxy)pyrido[3,2-d]pyrimidin-2-amineHCID 5769836290%

Reaction Steps

Potassium t-butoxide (4 mL, 4 mmol; 1 M in THF) was added to a suspension mixture of 6-chloro-4-[1,2,4]triazol-1-yl-pyrido[3,2-d]pyrimidin-2-ylamine (1 g, 4 mmol) and 2-methoxyethanol (0.32 mL, 4 mmol) in DCM (50 mL). After stirring at room temperature for 10 minutes, the mixture was diluted with DCM (100 mL) and washed with brine. The organic layer was dried over Na2SO4 and concentrated to afford the pure title compound as a beige solid (0.91 g, yield 90%) which was characterised as follows: MS (m/z) 225.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232278B2
Source datasetuspto-grants-2012_07
ORD IDord-68428d243fe846e992ebb25473db4967
Source noteuspto-grants-2012_07