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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715608Generated: October 30, 2026

Sulfamide → HCID 178527252, compound

https://huagongshe.com/reaction/715608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamideHCID 82267—
ReactantN-{[4-(aminomethyl)cyclohexyl]methyl}-8-(2-chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-amineHCID 89761016—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178527252HCID 17852725225%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of N-{[4-(aminomethyl)cyclohexyl]methyl}-8-(2-chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-amine (6.6 mg, 0.014 mmol, 1 eq.) in 5 mL of dioxane was added 10 mg of sulfamide. The reaction was heated to 80° C. and stirred 16 h. The reaction was concentrated in vacuo. The crude material was purified by silica gel column chromatography using 0-100% ethyl acetate/hexanes to yield 1.9 mg (25%) of N-{[4-({[8-(2-chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-yl]amino}methyl)cyclohexyl]methyl}aminosulfonamide. 1H NMR (300 MHz, METHANOL-d4) δ ppm 0.80-1.17 (m, 2 H) 1.21-1.79 (m, 6 H) 1.93 (br. s., 2 H) 3.00 (d, J=7.16 Hz, 2 H) 3.59 (br. s., 2 H) 7.19-7.69 (m, 8 H) 8.13-8.35 (m, 1 H), [M+H]+ 562.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187480B2
Source datasetuspto-grants-2015_11
ORD IDord-9f9937de5e7447169e58939489cb863a
Source noteuspto-grants-2015_11