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HRID 18484作成日:2026年10月24日

Methanol → [2-(2-amino-5-Methyl-sulfanyl-phenylamino)-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/ja/reaction/18484

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Ethyl AcetateHCID 8857—
反応物Sodium borohydrideHCID 4311764—
反応物[2-(5-Methyl-sulfanyl-2-nitro-phenylamino)-ethyl]-carbamic acid tert-butyl esterHCID 86615412—
触媒Nickel DichlorideHCID 24385—
溶媒DichloromethaneHCID 6344—
溶媒Sodium chloride; waterHCID 57417360—
生成物[2-(2-amino-5-Methyl-sulfanyl-phenylamino)-ethyl]-carbamic acid tert-butyl esterHCID 86615411—

反応条件

温度0 °C

反応手順

In a 500 mL round bottom flash equipped with a stir bar was charged with MeOH (200 mL), [2-(5-methyl-sulfanyl-2-nitro-phenylamino)-ethyl]-carbamic acid tert-butyl ester (5 g, 0.02 mol) and NiCl2 (19 g, 0.05 mol) and cooled to 0° C. NaBH4 (1.7 g, 0.05 mol) was added (in four equal portions) to the reaction mixture over a 1 h period. Once the addition was complete the reaction mixture was stirred for an additional 2 h. Brine (100 mL) and ethyl acetate (200 mL) were added to the reaction mixture. The heterogeneous mixture was transferred to a separatory funnel where the aqueous phase was separated and re-extracted with ethyl acetate (2×100 mL). The organic phases were combined and washed with H2O (3×100 mL), brine (100 mL), dried over MgSO4, filtered and concentrated under reduced pressure to give a black residue. The crude product was dissolved in 100 mL of CH2Cl2 and separated into two 100 mL round (50 mL in each) and both were concentrated under reduced pressure and used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741355B2
出典データセットuspto-grants-2010_06
ORD IDord-db976b0046da4a7a84077472e892d2a8
出典メモuspto-grants-2010_06