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

O,O-Dipyridin-2-yl carbonothioate → HCID 12049865, 화합물

HRID 1275674
노트
인쇄 미리보기

반응식

HRID 1275674 반응식
C1C=C(O[C:8](OC2N=CC=CC=2)=[S:9])N=CC=1.[NH2:17][C:18]1[CH:26]=[CH:25][CH:24]=[C:23]2[C:19]=1[C:20]([Cl:27])=[CH:21][NH:22]2>CN(C)C1C=CN=CC=1.C(Cl)Cl>[Cl:27][C:20]1[C:19]2[C:23](=[CH:24][CH:25]=[CH:26][C:18]=2[N:17]=[C:8]=[S:9])[NH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 719784O,O-Dipyridin-2-yl carbonothioateHCID 120498643-Chloro-1H-indol-4-amine

생성물 1

HCID 12049865HCID 12049865, 화합물수율 96%

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매HCID 6344Dichloromethane용매

실험 절차

4-Dimethylaminopyridine (0.031 g, 0.256 mmol) and di-2-pyridyl thionocarbonate (0.983 g, 4.23 mmol) are added to a solution of 4-amino-3-chloroindole (0.655 g, 2.82 mmol) in methylene chloride. The resulting mixture is stirred at room temperature for 1 hour. The volatile organics are removed by rotary evaporation and the crude residue is purified via silica gel column chromatography using 20% ethyl acetate/hexanes as the eluent. The appropriate fractions are combined and the solvents removed by rotary evaporation to yield 0.511 g of 3-chloro-4-isothiocyanatoindole as a yellow solid (96%).

후처리

  1. customThe volatile organics are removed by rotary evaporation
  2. customthe crude residue is purified via silica gel column chromatography
  3. customthe solvents removed by rotary evaporation

출처 및 근거

ORD 기록
ord-d478cbb1f30e4ee8845ca305ae261f85
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06162818

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트