Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418296Generated: October 27, 2026

Thionyl Chloride → Pyrazolo[1,5-a]pyrimidine-3-carbonyl chloride

https://huagongshe.com/reaction/418296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantPyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 1910189—
ProductPyrazolo[1,5-a]pyrimidine-3-carbonyl chlorideHCID 19623233107.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (11.73 g, 71.9 mmol) was suspended in thionyl chloride (36 mL, 493 mmol) and heated at 60° C. for 2 h. Formation of the acyl chloride was monitored as follows: a sample of the reaction mixture was evaporated and added to MeOH and formation of the corresponding methyl ester was detected by UPLC. Then thionyl chloride was removed under reduced pressure to obtain pyrazolo[1,5-a]pyrimidine-3-carbonyl chloride (14 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093249B2
Source datasetuspto-grants-2012_01
ORD IDord-6c8013a9a7fa4956a46e67507f5712aa
Source noteuspto-grants-2012_01