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

Sodium Hydroxide → 7-Thienylamino-1H-pyrazolo[4,3-b]pyridine

HRID 986746
노트
인쇄 미리보기

반응식

HRID 986746 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[NH:6][C:7]1[C:12](C(OCC)=O)=[CH:11][N:10]=[C:9]2[CH:18]=[N:19][NH:20][C:8]=12.[OH-].[Na+]>C(O)C>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]2[CH:18]=[N:19][NH:20][C:8]=12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 20156241Ethyl 7-thienylamino-1H-pyrazolo[4,3-b]pyridine-6-carboxylate

생성물 1

HCID 201562447-Thienylamino-1H-pyrazolo[4,3-b]pyridine

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ethyl 7-thienylamino-1H-pyrazolo[4,3-b]pyridine-6-carboxylate (0.600 g) was converted to the corresponding acid by heating under reflux with a 2% sodium hydroxide solution in ethanol (50 ml). The ethanol was removed under reduced pressure and the residue diluted with water (5 ml) and acidified to pH5 with dilute hydrochloric acid. The resulting acid was filtered off and dried, mp 255°-259° C.

후처리

  1. temperatureby heating
  2. customThe ethanol was removed under reduced pressure
  3. additionthe residue diluted with water (5 ml)
  4. filtrationThe resulting acid was filtered off
  5. customdried

출처 및 근거

ORD 기록
ord-795da91dd8ec4d3bba0d28a4380803d5
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04716160

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트