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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508864Generated: October 31, 2026

1-(4-Aminophenyl)methanesulfonamide → HCID 90113117, compound

https://huagongshe.com/reaction/1508864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Aminophenyl)methanesulfonamideHCID 10821407—
Reactant4-chloro-2-(3-chlorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidineHCID 21882677—
ProductHCID 90113117HCID 9011311758%

Reaction Steps

Following General Procedure A1, 4-chloro-2-(3-chlorophenyl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine (0.075 g, 0.28 mmol) was reacted with (4-aminophenyl)methanesulfonamide (0.058 g, 0.31 mmol) to afford the title compound (0.043 g, 58%) as a white solid. MW=414.91. 1H NMR (DMSO-d6, 300 MHz) δ 8.93 (s, 1H), 8.32-8.21 (m, 2H), 7.85 (d, J=8.6 Hz, 2H), 7.57-7.50 (m, 2H), 7.36 (d, J=8.6 Hz, 2H), 6.85 (s, 2H), 4.25 (s, 2H), 2.99-2.86 (m, 4H), 2.18-2.05 (m, 2H); APCI MS m/z 415 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-725e538c53884e8b890d6874b0c644a4
Source noteuspto-grants-2015_12