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

Water → 3-Ethoxythieno[2,3-b]pyrazine-6-carboxylic acid

HRID 1184914
노트
인쇄 미리보기

반응식

HRID 1184914 반응식
Cl[C:2]1[N:7]=[C:6]2[S:8][C:9]([C:11]([O:13]C)=[O:12])=[CH:10][C:5]2=[N:4][CH:3]=1.[OH-].[Na+].O.C1C[O:21][CH2:20][CH2:19]1>CO>[CH2:20]([O:21][C:2]1[N:7]=[C:6]2[S:8][C:9]([C:11]([OH:13])=[O:12])=[CH:10][C:5]2=[N:4][CH:3]=1)[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 86680178Methyl 3-chlorothieno[2,3-b]pyrazine-6-carboxylate

생성물 1

HCID 671256133-Ethoxythieno[2,3-b]pyrazine-6-carboxylic acid수율 100%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of methyl 3-chlorothieno[2,3-b]pyrazine-6-carboxylate 92 (0.044 mmol, 10 mg) in methanol 250 uL and THF 250 uL was added sodium hydroxide 2N in water (0.219 mmol, 109 μA) and stirred overnight at rt. The reaction mixture was quenched in 2N HCl and extracted with CH2Cl2/methanol (9/1). The organic layer was dried and concentrated under reduced pressure to give 3-ethoxythieno[2,3-b]pyrazine-6-carboxylic acid 97 (9.3 mg, 100%).

후처리

  1. customThe reaction mixture was quenched in 2N HCl
  2. extractionextracted with CH2Cl2/methanol (9/1)
  3. customThe organic layer was dried
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-57acba7d6d4b4dd6a83c3f0e9bd0900d
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08669256B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트