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HRID 45574作成日:2026年10月24日

Ammonia → 2,2-difluoro-2-pyridin-2-yl-ethylamine benzenesulphonate, (1:1 salt)

https://huagongshe.com/ja/reaction/45574

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Sodium IodideHCID 5238—
反応物Benzenesulfonic AcidHCID 7371—
反応物2,2-Difluoro-2-pyridin-2-ylethyl 4-methylbenzenesulfonateHCID 58249642—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Isopropyl AcetateHCID 7915—
生成物2,2-difluoro-2-pyridin-2-yl-ethylamine benzenesulphonate, (1:1 salt)HCID 7835786349.5%

反応条件

温度80 °C

反応手順

10 g of 2,2-Difluoro-2-pyridin-2-ylethyl 4-methylbenzenesulfonate (J) obtained in step 3, 5 g of NaI, 20 mL of DMSO and 90 mL of aqueous ammonia were taken in a 500 mL autoclave vessel. The reaction mixture was heated to 80° C. and a pressure of 15 to 17 kg of ammonia maintained for 30-40 hours. The volume of the reaction mass was reduced by vacuum distillation. The RM was washed with 60 mL of IPE. The pH of the RM was adjusted to 10-14 by adding a 50% NaOH solution and extracted three times with 60 mL of MDC. The combined MDC layers were washed with brine, dried over sodium sulphate and distilled under vacuum (crude weight=8 g). The crude mass obtained was dissolved with 10 mL of MDC, and to this 4.5 g benzene sulphonic acid (BSA) dissolved in 30 mL isopropyl acetate (IPAc) was added dropwise over a period of 30 minutes with stirring at RT. The RM was stirred for 30 minutes at RT. The solid obtained was filtered and washed with IPAc and dried under vacuum, resulting in 5 g of the titled compound (Yield=49.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541580B2
出典データセットuspto-grants-2013_09
ORD IDord-ac1aafe395f44b6fa336ed0ef1904144
出典メモuspto-grants-2013_09