Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536241Generated: October 29, 2026

3-chloro-N,N-dimethylpropane-1-sulfonamide → HCID 178486161, compound

https://huagongshe.com/reaction/536241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-chloro-N,N-dimethylpropane-1-sulfonamideHCID 10035328—
ReactantN-(7-hydroxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)pyridine-3-carboxamideHCID 178522515—
ProductHCID 178486161HCID 178486161—

Reaction Steps

The procedure used for the preparation of Example 1 was used to prepare the title compound from N-(7-hydroxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)nicotinamide (Intermediate C) and 3-chloro-N,N-dimethylpropane-1-sulfonamide (Intermediate F). High vacuum drying at 60° C. gave the title compound (44 mg, 39%): HPLC MS RT=0.68 min, MH+=457.3; 1H NMR (DMSO-d6+2 drops TFA-d) δ: 2.27 (2H, bs), 2.84 (6H, s), 3.36-3.37 (2H, m), 4.31 (2H, bs), 4.43 (2H, bs), 4.62 (2H, bs), 7.59-7.61 (1H, m), 7.71 (1H, bs), 7.83-7.86 (1H, m), 7.97-7.98 (1H, m), 8.89 (1H, bs), 9.00 (1H, m), 9.47 (1H, bs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859572B2
Source datasetuspto-grants-2014_10
ORD IDord-b1e3982288a7426eb17e76c56f67ad5c
Source noteuspto-grants-2014_10