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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840199Generated: October 30, 2026

2-Butanamine, 3,3-dimethyl- → 3-[3,5-Bis(trifluoromethyl)phenylamino]-2-(4-chlorophenylsulfonyl)-3-(1,2,2-trimethylpropylamino)-2-propenenitrile

https://huagongshe.com/reaction/840199

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butanamine, 3,3-dimethyl-HCID 520907—
Reactant3-(3,5-Bis(trifluoromethyl)phenylamino)-2-(4-chlorophenylsulfonyl)-3-methylsulfanyl-2-propenenitrileHCID 86583731—
Product3-[3,5-Bis(trifluoromethyl)phenylamino]-2-(4-chlorophenylsulfonyl)-3-(1,2,2-trimethylpropylamino)-2-propenenitrileHCID 7655992268%

Reaction Steps

3-(3,5-Bis(trifluoromethyl)phenylamino)-2-(4-chloro-phenylsulfonyl)-3-methylsulfanyl-2-propenenitrile (0.300 g, 0.6 mmol) was stirred in 1,2,2-trimethylpropylamine (1 ml) for 19 h at 75° C. under nitrogen. The reaction mixture was concentrated and the residue dissolved in DCM, washed twice with 1N aqueous HCl and once with water. The organic phase was dried (sodium sulfate) and concentrated. The residue was crystallised from ethyl acetate/heptane 1:3 to give 225 mg (68%) of the title compound. Mp 155.5-158.5° C. 1H NMR (300 MHz, CDCl3): δ=0.9 (s, 9H), 1.0 (d, 3H), 3.0 (m, 1H), 7.40 (s, 2H), 7.50 (d, 2H), (s, 1H), 7.82 (d, 2H); MA calc for C23H22ClF6N3O2S: C, 49.87%; H, 4.00%; N, 7.59%. Found: C, 49.86%; H, 4.29%; N, 7.55%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365609B1
Source datasetuspto-grants-2002_04
ORD IDord-4aeb4a10ebc84e1aadcc6aae310cf6f7
Source noteuspto-grants-2002_04