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

Sodium Hydroxide → HCID 86701047, 화합물

HRID 715735
노트
인쇄 미리보기

반응식

HRID 715735 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:12]2[N:13]=[C:14]([S:17][CH:18]([CH2:24][CH3:25])[C:19]([O:21]CC)=[O:20])[CH:15]=[CH:16][C:11]2=[N:10][N:9]=1.[OH-].[Na+]>O1CCOCC1>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:12]2[N:13]=[C:14]([S:17][CH:18]([CH2:24][CH3:25])[C:19]([OH:21])=[O:20])[CH:15]=[CH:16][C:11]2=[N:10][N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 86701046HCID 86701046, 화합물

생성물 1

HCID 86701047HCID 86701047, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

To a solution of ethyl 2-((3-(2-fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)thio)butanoate (1 mmol) in dioxane (3 mL) was added 0.5 ml of sodium hydroxide (2N), and the reaction mixture was stirred at room temperature. After 2 hours, the mixture was evaporated to dryness, and the obtained residue dissolved in water (2 mL) and then acidified with an hydrochloric acid solution. The resulting precipitate was filtered, washed with water, and dried to give 2-((3-(2-fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)thio)butanoic acid.

후처리

  1. customthe mixture was evaporated to dryness
  2. dissolutionthe obtained residue dissolved in water (2 mL)
  3. filtrationThe resulting precipitate was filtered
  4. washwashed with water
  5. customdried

출처 및 근거

ORD 기록
ord-212673257a9e483fbcda49c7e081696e
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187484B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트