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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → (E)-3-(6-aminopyrid-3-yl)acrylic acid hydrochloride

HRID 633922
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반응식

HRID 633922 반응식
[NH2:1][C:2]1[N:7]=[CH:6][C:5](/[CH:8]=[CH:9]/[C:10]([O:12]C(C)(C)C)=[O:11])=[CH:4][CH:3]=1.FC(F)(F)C(O)=O.[ClH:24]>C(Cl)Cl.O1CCOCC1>[ClH:24].[NH2:1][C:2]1[N:7]=[CH:6][C:5](/[CH:8]=[CH:9]/[C:10]([OH:12])=[O:11])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 6422Trifluoroacetic acidHCID 57777730Tert-butyl 3-(6-aminopyridin-3-yl)prop-2-enoate

생성물 1

HCID 66967187(E)-3-(6-aminopyrid-3-yl)acrylic acid hydrochloride수율 76%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 312751,4-Dioxane용매

실험 절차

To a solution of tert-butyl(2E)-3-(6-aminopyridin-3-yl)acrylate (380 mg, 1.73 mmol; which may be prepared as described in Step 1) in DCM (3.45 mL) under Argon was added trifluoroacetic acid (3.45 mL). The mixture was stirred at room temperature for 1 h, then HCl 4N in dioxane (6.9 mL) was added. A beige solid started precipitating at the half of the addition. After concentration, the solid was triturated in Et2O, filtered, rinsed with Et2O and dried under vacuum to give the title compound as a beige solid (265 mg, 76%).

후처리

  1. customA beige solid started precipitating at the half of the addition
  2. concentrationAfter concentration
  3. customthe solid was triturated in Et2O
  4. filtrationfiltered
  5. washrinsed with Et2O
  6. customdried under vacuum

출처 및 근거

ORD 기록
ord-66bf979289be4381900ec5d4788c634f
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09321769B2

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