Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157553Generated: October 29, 2026

2-Thiopheneacetyl chloride → HCID 16122935, compound

https://huagongshe.com/reaction/1157553

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiopheneacetyl chlorideHCID 162362—
ReactantHCID 59511429HCID 59511429—
ProductHCID 16122935HCID 1612293544%

Reaction Steps

The title compound was prepared from 4-[2-(3-aminophenyl)pyrazolo[1,5-a]pyridin-3-yl]-N-(3-{[2-(1-pyrrolidinyl)ethyl]oxy}phenyl)-2-pyrimidinamine and 2-thiopheneacetyl chloride using acylation conditions described in Example 1, Step F, and purification via column chromatography using a 0-20% gradient of EtOAc/MeOH w/NH4OH to generate the product in 44% yield. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.6 (s, 4H) 2.7 (s, 3H) 3.8 (s, 2H) 4.0 (t, J=6.0 Hz, 2H) 6.5 (m, 2H) 6.9 (m, 2H) 7.1 (m, 3H) 7.2 (m, 2H) 7.4 (m, 2H) 7.4 (m, 1H) 7.5 (t, J=2.3 Hz, 1H) 7.7 (m, 1H) 7.9 (d, J=1.8 Hz, 1H) 8.2 (d, J=5.3 Hz, 1H) 8.5 (s, 1H) 8.8 (d, J=7.0 Hz, 1H) 9.5 (s, 1H) 10.3 (s, 1H). ES-LC/MS m/z 616 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807673B2
Source datasetuspto-grants-2010_10
ORD IDord-729e951cfb3246d08699a9fc683f66a4
Source noteuspto-grants-2010_10