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HRID 5828생성일: 2026년 10월 24일

1-Amino-2-naphthalenethiol → 3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one

https://huagongshe.com/ko/reaction/5828

반응식

참여 물질

역할이름HCID투입량
반응물1-Amino-2-naphthalenethiolHCID 113314—
반응물Sodium AcetateHCID 517045—
반응물Sodium borohydrideHCID 4311764—
반응물Methyl 2-bromo-2-(4-chlorophenyl)acetateHCID 10777987—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
생성물3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-oneHCID 1898444086%

반응 단계

To a solution of 1-amino-2-naphthalenethiol (27.81 g) in ethanol (500 ml) is added sodium borohydride (11.35 g) at room temperature. The mixture is stirred for 20 minutes, and thereto is added dropwise acetic acid (200 ml) and is further added sodium acetate (24.6 g). To the mixture is further added dropwise methyl α-bromo-4-chlorophenylacetate (46.8 g), and the mixture is sitrred at room temperature under argon overnight. The reaction mixture is poured into ice water and the resulting precipitate is separated by filtration, washed, dried and recrystallized from tetrahydrofuran-n-hexane to give 3-(4-chlorophenyl)-1H-naphtho-[2,1-b][1,4]thiazin-2(3H)-one (44.45 g, yield 82.6%) as crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246929
출처 데이터셋uspto-grants-1993_09
ORD IDord-d1e1ce17b0b34812b37a771e23bf789c
출처 메모uspto-grants-1993_09