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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536238Generated: October 30, 2026

1-((3-Chloropropyl)sulfonyl)-4-methylpiperazine → HCID 178481109, compound

https://huagongshe.com/reaction/536238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((3-Chloropropyl)sulfonyl)-4-methylpiperazineHCID 10243385—
ReactantN-(7-hydroxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)pyridine-3-carboxamideHCID 178522515—
ProductHCID 178481109HCID 178481109—

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 1-[(3-chloropropyl)sulfonyl]-4-methylpiperazine (Intermediate D). High vacuum drying at 60° C. gave the title compound (72 mg, 57%): HPLC MS RT=1.22 min, MH+=512.2; 1H NMR (DMSO-d6+2 drops TFA-d) δ: 2.26-2.31 (2H, m), 2.82 (3H, s), 3.11-3.21 (4H, m), 3.45-3.50 (4H, m), 3.83-3.87 (2H, m), 4.27-4.34 (2H, m), 4.42 (2H, t), 4.58-4.65 (2H, m), 7.60 (1H, t), 7.73 (1H, d), 7.85 (1H, d), 7.94 (1H, dd), 8.86 (1H, d), 9.00 (1H, dd), 9.48 (1H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859572B2
Source datasetuspto-grants-2014_10
ORD IDord-7c5c1fb74c6045b59bc8fb62e844cf25
Source noteuspto-grants-2014_10