Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238177Generated: October 26, 2026

5-bromo-N-(2-(dimethylamino)ethyl)thiophene-2-sulfonamide → 5-[5-(4-Chloro-3-methyl-phenyl)-7-difluoromethyl-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-thiophene-2-sulfonic acid (2-dimethylamino-ethyl)-amide

https://huagongshe.com/reaction/2238177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-bromo-N-(2-(dimethylamino)ethyl)thiophene-2-sulfonamideHCID 8716799—
Reactant5-(4-Chloro-3-methyl-phenyl)-7-difluoromethyl-3-ethynyl-pyrazolo[1,5-a]pyrimidineHCID 86608084—
Product5-[5-(4-Chloro-3-methyl-phenyl)-7-difluoromethyl-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-thiophene-2-sulfonic acid (2-dimethylamino-ethyl)-amideHCID 67000752—

Reaction Steps

The title compound was prepared from 5-(4-chloro-3-methyl-phenyl)-7-difluoromethyl-3-ethynyl-pyrazolo[1,5-a]pyrimidine (example C.16) (159 mg, 0.5 mmol) and 5-bomo-thiophene-2-sulfonic acid (2-dimethylamino-ethyl)-amide (example B.49) (157 mg, 0.5 mmol) according to general procedure II. Obtained as a yellow solid (200 mg, 73%). MS (ISN) 548.1 [(M−H)−]; mp 149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718661B2
Source datasetuspto-grants-2010_05
ORD IDord-b60890b2e7b84d75af00680a8332d982
Source noteuspto-grants-2010_05