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

Hydrochloric Acid → 6-(Furan-2-yl)-2-oxo-1,2-dihydropyridine-3-carbonitrile

HRID 353213
노트
인쇄 미리보기

반응식

HRID 353213 반응식
CN(C)[CH:3]=[CH:4][C:5]([C:7]1[O:8][CH:9]=[CH:10][CH:11]=1)=O.[C:13]([CH2:15][C:16]([NH2:18])=[O:17])#[N:14].C(=O)([O-])[O-].[K+].[K+].Cl>CS(C)=O.O>[O:8]1[CH:9]=[CH:10][CH:11]=[C:7]1[C:5]1[NH:18][C:16](=[O:17])[C:15]([C:13]#[N:14])=[CH:3][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 7898CyanoacetamideHCID 11430Potassium CarbonateHCID 535936HCID 535936, 화합물

생성물 1

HCID 27470886-(Furan-2-yl)-2-oxo-1,2-dihydropyridine-3-carbonitrile수율 77%

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 962
Water
용매

반응 조건

온도
130 °C

실험 절차

A suspension of 3-(dimethylamino)-1-(2-furyl)-2-propen-1-one (15.0 g, 90.9 mmol), 2-cyanoacetamide (8.5 g, 101 mmol) and potassium carbonate (38.0 g, 275 mmol) in dimethyl sulfoxide (80 ml) was stirred at 120 to 140° C. for 21 hours. After cooling as it was, the reaction mixture was diluted with water. After adjusting to pH 3 with conc. hydrochloric acid, the resulting solid was collected by filtration and washed with water, to give the title compound (13.0 g, 77%) as a brown solid.

후처리

  1. temperatureAfter cooling as it
  2. filtrationthe resulting solid was collected by filtration
  3. washwashed with water

출처 및 근거

ORD 기록
ord-e778b8b6f0414bec9b84149b89bbbd63
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06750232B2

반응 노트

불러오는 중…