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Pyridine → Zsb11

HRID 1906258
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HRID 1906258 반응식
[OH:1][CH2:2][N:3]1[C:8](=[O:9])[CH2:7][N:6]([CH2:10][CH2:11][N:12]2[CH2:17][C:16](=[O:18])[N:15]([CH2:19][OH:20])[C:14](=[O:21])[CH2:13]2)[CH2:5][C:4]1=[O:22].N1C=CC=CC=1.[C:29](OC(=O)C)(=[O:31])[CH3:30].[C:36](OCC)(=[O:38])[CH3:37]>>[C:29]([O:20][CH2:19][N:15]1[C:14](=[O:21])[CH2:13][N:12]([CH2:11][CH2:10][N:6]2[CH2:7][C:8](=[O:9])[N:3]([CH2:2][O:1][C:36](=[O:38])[CH3:37])[C:4](=[O:22])[CH2:5]2)[CH2:17][C:16]1=[O:18])(=[O:31])[CH3:30]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 1049PyridineHCID 7918Acetic AnhydrideHCID 8857Ethyl AcetateHCID 13532751HCID 13532751, 화합물

생성물 1

HCID 3062668Zsb11수율 70.5%

실험 절차

A mixture of 1,2-bis(4-hydroxymethyl-3,5-dioxopiperazin-1-yl)ethane (1.50 g, 4.8 m mol), pyridine (10 ml) and acetic anhydride (5 ml, 52.9 m mol) was stirred for 12 hours at room temperature. The reaction mixture was diluted with ethyl acetate (20 ml) and the resulting crystals were collected and washed with ethyl acetate and successively with ether and was dried under reduced pressure to give the titled compound (1.34 g; yield 70.5%).

후처리

  1. customthe resulting crystals were collected
  2. washwashed with ethyl acetate and successively with ether
  3. customwas dried under reduced pressure

출처 및 근거

ORD 기록
ord-7d3b2737fbe24575ac718aa6fe93a6f8
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04650799

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