Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536261Generated: October 28, 2026

1-(Chloromethyl)-4-methanesulfonylbenzene → HCID 178432763, compound

https://huagongshe.com/reaction/536261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Chloromethyl)-4-methanesulfonylbenzeneHCID 123530—
ReactantHCID 178487303HCID 178487303—
ProductHCID 178432763HCID 178432763—

Reaction Steps

The procedure used for the preparation of Example 24, Step 2 was used to prepare the title compound from N-(8-hydroxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)-2,4-dimethyl-1,3-thiazole-5-carboxamide (Step 1) and 1-(chloromethyl)-4-(methylsulfonyl)benzene (15 mg, 51%). TLC: Rf 0.93 in 10% MeOH/CH2Cl2, HPLC MS RT=2.27 min, MH+=510.1; 1H NMR (DMSO-d6) δ: 2.80 (3H, s), 2.86 (3H, s), 3.39 (3H, s), 4.30-4.35 (2H, m), 4.50-4.54 (2H, m), 5.56 (2H, s), 7.39 (1H, d), 7.87 (2H, d), 7.95 (1H, s), 8.11 (2H, d), 8.50 (1H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859572B2
Source datasetuspto-grants-2014_10
ORD IDord-e0306a45323240d08e4cb27afd32c216
Source noteuspto-grants-2014_10