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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099111Generated: October 31, 2026

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

https://huagongshe.com/reaction/1099111

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 tert-butoxide (4 mL; 1M in THF) was added to a suspension of 6-Chloro-4-[1,2,4]triazol-1-yl-pyrido[3,2-d]pyrimidin-2-ylamine (1 g) and 2-methoxyethanol (0.32 mL) 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 6-chloro-4-(2-methoxy-ethoxy)-pyrido[3,2-d]pyrimidin-2-ylamine as a beige solid (0.91 g, yield: 90%) which was characterized by its mass spectrum as follows: MS (m/z) 225.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143394B2
Source datasetuspto-grants-2012_03
ORD IDord-dee356fc3ffb48f18ebf074c70b72c36
Source noteuspto-grants-2012_03