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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Isonicotinic Acid → 2,5-Pyrrolidinedione, 1-[(4-pyridinylcarbonyl)oxy]-

HRID 1368953
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HRID 1368953 반응식
[C:1]([OH:9])(=[O:8])[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.O[N:11]1[C:15](=[O:16])[CH2:14][CH2:13][C:12]1=[O:17]>C1COCC1>[C:1]([O:9][N:11]1[C:15](=[O:16])[CH2:14][CH2:13][C:12]1=[O:17])(=[O:8])[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5922Isonicotinic AcidHCID 80170N-Hydroxysuccinimide

생성물 1

HCID 27548292,5-Pyrrolidinedione, 1-[(4-pyridinylcarbonyl)oxy]-수율 98.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of isonicotinic acid (3 g), N-hydroxysuccinimide (2.79 g) and N,N-dicyclohexylcarbodiimide (5.52 g) was stirred in THF (200 mL) for 16 hours. The solid was filtered off and the solvent evaporated under reduced pressure. The residue was triturated with ethyl acetate and more solid filtered off. The filtrates were concentrated under reduced pressure gave 2,5-dioxopyrrolidin-1-yl isonicotinate (5.27 g). MS: 221 [MH]+.

후처리

  1. filtrationThe solid was filtered off
  2. customthe solvent evaporated under reduced pressure
  3. customThe residue was triturated with ethyl acetate and more solid
  4. filtrationfiltered off
  5. concentrationThe filtrates were concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-484efae79cfc4124ad2aa9afdd3a06d9
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06576630B1

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