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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243337Generated: October 26, 2026

Methyl iodide → 5-Chloro-1-methyl-1H-pyrazolo[4,3-D]pyrimidine

https://huagongshe.com/reaction/243337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant5-Chloro-1H-pyrazolo(4,3-d)pyrimidineHCID 59796947—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-1-methyl-1H-pyrazolo[4,3-D]pyrimidineHCID 7174311514%

Reaction Conditions

Temperature0 °C

Reaction Steps

Potassium t-butoxide (1.68 g, 14.67 mmol, 1.14 equiv) was added to a solution of 5-chloro-1H-pyrazolo[4,3-d]pyrimidine (2.1 g, 12.91 mmol, 1.00 equiv, 95%) in tetrahydrofuran (50 mL) at 0° C. After the reaction mixture was stirred at 0° C. for 30 min, iodomethane (3 g, 20.71 mmol, 1.60 equiv, 98%) was added dropwise at 0° C. The resulting solution was stirred for 4.5 h at room temperature and then concentrated under vacuum. The residue was loaded onto a silica gel column and eluted with dichloromethane/ethyl acetate (10/1) to give 300 mg (14%) of 5-chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-2523d93b75e54bcd8bf8b688e04053c3
Source noteuspto-grants-2014_02