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HRID 279109作成日:2026年10月27日

(R)-3,3-Dimethyl-2-aminobutane → (R)-3-[3,5-bis(trifluoromethyl)phenylamino]-2-(4-chlorophenylsulfonyl)-3-(1,2,2-trimethylpropylamino)-2-propenenitrile

https://huagongshe.com/reaction/279109

反応式

関与物質

役割名称HCID仕込み量
反応物(R)-3,3-Dimethyl-2-aminobutaneHCID 5324845—
反応物3-(3,5-Bis(trifluoromethyl)phenylamino)-2-(4-chlorophenylsulfonyl)-3-methylsulfanyl-2-propenenitrileHCID 86583731—
生成物(R)-3-[3,5-bis(trifluoromethyl)phenylamino]-2-(4-chlorophenylsulfonyl)-3-(1,2,2-trimethylpropylamino)-2-propenenitrileHCID 8658373739%

反応手順

3-(3,5-Bis(trifluoromethyl)phenylamino)-2-(4-chloro-phenylsulfonyl)-3-methylsulfanyl-2-propenenitrile (0.300 g, 0.6 mmol) was stirred in (R)-1,2,2-trimethylpropylamine (1 ml) for 17 h at 75° C. under nitrogen. Work-up as described in Example 17, 2) gave 131 mg (39%) of the title compound. Mp 164-165° C. 1H NMR (200 MHz, CDCl3): δ=0.9 (s, 9H), 1.0 (d, 3H), 3.0 (m, 1H), 7.37 (s, 2H), 7.50 (d, 2H), 7.68 (s, 1H), 7.80 (d, 2H); Analysis: calc. for C23H22ClF6N3O2S: C, 49.87%; H, 4.00%; N, 7.59%. Found: C, 49.95%; H, 4.15%; N, 7.48%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362205B1
出典データセットuspto-grants-2002_03
ORD IDord-d85db34c1a024a34b90c800ee1f2d281
出典メモuspto-grants-2002_03