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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18484생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Ethyl AcetateHCID 8857—
반응물Sodium borohydrideHCID 4311764—
반응물[2-(5-Methyl-sulfanyl-2-nitro-phenylamino)-ethyl]-carbamic acid tert-butyl esterHCID 86615412—
촉매Nickel DichlorideHCID 24385—
용매DichloromethaneHCID 6344—
용매Sodium chloride; waterHCID 57417360—
생성물[2-(2-amino-5-Methyl-sulfanyl-phenylamino)-ethyl]-carbamic acid tert-butyl esterHCID 86615411—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741355B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-db976b0046da4a7a84077472e892d2a8
출처 메모uspto-grants-2010_06