Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Chlorosulfonyl isocyanate → 6-methoxy-2-methyl-1H-indole-3-carbonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Chlorosulfonyl isocyanate | HCID 70918 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 6-methoxy-2-methyl-1H-indole | HCID 10844709 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 6-methoxy-2-methyl-1H-indole-3-carbonitrile | HCID 13904640 | 81% |
반응 단계
To a solution of 6-methoxy-2-methyl-1H-indole (3.9 g, 24 mmol) in acetonitrile (200 mL) and DMF (20 mL) is added dropwise a solution of ClSO2NCO (4 mL, 1.3 eq.) in acetonitrile (31 mL) at 0° C. After the addition, the mixture is stirred at room temperature for 3 h. Then it is poured into ice water and saturated NaHCO3 is added to it until it becomes basic. The aqueous phase is extracted with CH2Cl2 and then evaporated. The residue is purified with flash column chromatography on silica gel using EtOAc/petroleum ether (1/5) as eluent to yield 81% of 6-methoxy-2-methyl-1H-indole-3-carbonitrile.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07868037B2 |
| 출처 데이터셋 | uspto-grants-2011_01 |
| ORD ID | ord-a3b2adcd5e7a4039b8a70e9d60a9474a |
| 출처 메모 | uspto-grants-2011_01 |