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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850704Generated: October 30, 2026

HCID 86720889, compound → 2-amino-6-fluoro-N-(3-methyl-4-(pyrrolidin-1-yl)isothiazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

https://huagongshe.com/reaction/1850704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86720889HCID 86720889—
Reactant3-Methyl-4-(pyrrolidin-1-yl)isothiazol-5-amineHCID 90412425—
SolventPyridineHCID 1049—
Product2-amino-6-fluoro-N-(3-methyl-4-(pyrrolidin-1-yl)isothiazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamideHCID 85472930—

Reaction Conditions

Temperature105 °C

Reaction Steps

A mixture of (6-chlorobenzotriazol-1-yl) 2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carboxylate (140.4 mg, 0.4038 mmol), 3-methyl-4-(pyrrolidin-1-yl)isothiazol-5-amine (37 mg, 0.2019 mmol) (synthesized according to preparation 13) in pyridine (3 mL) was heated at 105° C. for 24 h. The mixture was concentrated in vacuo and the residue was purified by fractionlynx. The clean fractions were combined and freeze dried to yield 2-amino-6-fluoro-N-(3-methyl-4-(pyrrolidin-1-yl)isothiazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide as a pale yellow solid. (25 mg, 26%). MS (ES+) 362.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957078B2
Source datasetuspto-grants-2015_02
ORD IDord-6f6b886918374738a74307029b18fe69
Source noteuspto-grants-2015_02