홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

O,O-Dipyridin-2-yl carbonothioate → 6-Isothiocyanato-7-methylindole

HRID 1275657
노트
인쇄 미리보기

반응식

HRID 1275657 반응식
[NH2:1][C:2]1[C:10]([CH3:11])=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1.C1C=C(O[C:19](OC2N=CC=CC=2)=[S:20])N=CC=1>C(Cl)Cl>[N:1]([C:2]1[C:10]([CH3:11])=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1)=[C:19]=[S:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 719784O,O-Dipyridin-2-yl carbonothioateHCID 158963787-methyl-1H-indol-6-amine

생성물 1

HCID 158963796-Isothiocyanato-7-methylindole수율 70%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 6-amino-7-methylindole (1.0 g, 6.84 mmol) in methylene chloride (50 mL) is added di-2-pyridyl thionocarbonate (1.59 g, 6.84 mmol). The resulting solution is stirred at room temperature for two hours followed by removal of the methylene chloride by rotary evaporation. The crude material is purified via silica gel column chromatography using 10% ethyl acetate/hexane as the eluting solvent. The product containing fractions are combined and the solvents removed by rotary evaporation to yield 0.90 g of 6-isothiocyanato-7-methylindole as a white solid (70% yield).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customfollowed by removal of the methylene chloride by rotary evaporation
  2. customThe crude material is purified via silica gel column chromatography
  3. additionThe product containing fractions
  4. customthe solvents removed by rotary evaporation

출처 및 근거

ORD 기록
ord-d60a1724c27447bea73ce600b591400c
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06162818

반응 노트

불러오는 중…