Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-Amino-2-naphthalenethiol → 3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-Amino-2-naphthalenethiol | HCID 113314 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | Methyl 2-bromo-2-(4-chlorophenyl)acetate | HCID 10777987 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one | HCID 18984440 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05246929 |
| 출처 데이터셋 | uspto-grants-1993_09 |
| ORD ID | ord-d1e1ce17b0b34812b37a771e23bf789c |
| 출처 메모 | uspto-grants-1993_09 |