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

Potassium Carbonate → 5-Acetyl-2-aminothieno[3,2-b]thiophene-3-carbonitrile

HRID 1905459
노트
인쇄 미리보기

반응식

HRID 1905459 반응식
[NH2:1][C:2]1[S:3][C:4]([CH:10]=O)=[C:5](Cl)[C:6]=1[C:7]#[N:8].C(=O)([O-])[O-].[K+].[K+].[CH2:18]([SH:22])[C:19]([CH3:21])=[O:20]>CN(C)C=O>[C:19]([C:18]1[S:22][C:5]2[C:6]([C:7]#[N:8])=[C:2]([NH2:1])[S:3][C:4]=2[CH:10]=1)(=[O:20])[CH3:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 5201441-Mercapto-2-propanoneHCID 27376122-Amino-4-chloro-5-formyl-3-thiophenecarbonitrile

생성물 1

HCID 140473255-Acetyl-2-aminothieno[3,2-b]thiophene-3-carbonitrile수율 81%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
60 °C

실험 절차

A mixture of 18.7 parts of 2-amino-4-chloro-3-cyano-5-formylthiophene, 13.8 parts of potassium carbonate and 80 parts of N,N-dimethylformamide was introduced first, and 9 parts of acetonylmercaptan were then added. After the exothermic reaction had died down, the mixture was heated at 60° C. for 1 hour and then discharged onto water. The precipitate was filtered off with suction, washed with water and dried. This gave 17.9 parts (81% of theory) of 5-acetyl-2-amino-3-cyanothieno[3,2-b]thiophene.

후처리

  1. additionwas introduced first
  2. customAfter the exothermic reaction
  3. filtrationThe precipitate was filtered off with suction
  4. washwashed with water
  5. customdried

출처 및 근거

ORD 기록
ord-978a397eb93e43c3971ae9a844a69f10
출처 데이터셋
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04843153

반응 노트

불러오는 중…