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

Hydrochloric Acid → Methyl 5-(hydroxymethyl)pyrazine-2-carboxylate

HRID 1524643
노트
인쇄 미리보기

반응식

HRID 1524643 반응식
[CH:1]([C:3]1[N:4]=[CH:5][C:6]([C:9]([O:11][CH3:12])=[O:10])=[N:7][CH:8]=1)=[O:2].[BH4-].[Na+].CO.Cl>C1COCC1.[Cl-].[Na+].O>[OH:2][CH2:1][C:3]1[N:4]=[CH:5][C:6]([C:9]([O:11][CH3:12])=[O:10])=[N:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 4311764Sodium borohydrideHCID 44515461Methyl 5-formylpyrazine-2-carboxylate

생성물 1

HCID 66869530Methyl 5-(hydroxymethyl)pyrazine-2-carboxylate수율 52.4%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of methyl 5-formylpyrazine-2-carboxylate (2.47 g) in THF (20 mL) was added sodium borohydride (170 mg) portionwise over 10 mins. After stirring for 1 h, methanol (10 mL) was added. The reaction mixture was stirred for a further 20 mins, and then HCl (1 N, aq., 20 mL) and brine (20 mL) were added. The mixture was extracted with EtOAc (3×40 mL) and the combined organic portions dried over MgSO4 and evaporated to afford the title compound (1.31 g). 1H NMR (400 MHz, CDCl3) δ ppm 4.07 (s, 3H), 4.98 (br. s., 2H), 8.80 (s, 1H), 9.27 (s, 1H)

후처리

  1. stirringThe reaction mixture was stirred for a further 20 mins
  2. extractionThe mixture was extracted with EtOAc (3×40 mL)
  3. dry with materialthe combined organic portions dried over MgSO4
  4. customevaporated

출처 및 근거

ORD 기록
ord-77de3f97c1be40858d77f8606f9dae41
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09079914B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 57417360
Sodium chloride; water
용매