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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279126Generated: October 26, 2026

2-Butanamine, 3,3-dimethyl- → 2-(4-Chlorophenylsulfonyl)-3-(3-cyanophenylamino)-3-(1,2,2-trimethylpropylamino)-2-propenenitrile

https://huagongshe.com/reaction/279126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butanamine, 3,3-dimethyl-HCID 520907—
Reactant2-(4-Chlorophenylsulfonyl)-3-(3-cyanophenylamino)-3-methylsulfanyl-2-propenenitrileHCID 70150628—
Product2-(4-Chlorophenylsulfonyl)-3-(3-cyanophenylamino)-3-(1,2,2-trimethylpropylamino)-2-propenenitrileHCID 7015033325%

Reaction Steps

2-(4-Chlorophenylsulfonyl)-3-(3-cyanophenylamino)-3-methylsulfanyl-2-propenenitrile (0.300 g, 0.6 mmol) was stirred in 2-amino-3,3-dimethylbutane (1 ml) for 48 h at 100° C. under nitrogen in a sealed flask. The reaction mixture was concentrated and the residue dissolved in dichloromethane, washed twice with 1N aqueous HCl, once with brine, and once with water. The organic phase was dried (sodium sulphate) and concentrated. The residue was trituated with ether to afford a white crystalline substance which was further purified by flash chromatography(SiO2) using heptane/ethyl acetate (1:1) to yield 85 mg(25%) of the title compound. Mp 80-82 ° C. 1H NMR (200 MHz, CDCl3): δ=0.90 (s, 9H), 1.02 (d, 3H), 3.02 (m, 1H), 7.27 (s, 2H), 7.47 (d, 2H), 7.51 (d,2H), 7.81 (d, 2H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362205B1
Source datasetuspto-grants-2002_03
ORD IDord-6564973660d046d38d3c64ce3fc6378c
Source noteuspto-grants-2002_03