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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 22283192, 화합물 → HCID 178488787, 화합물

HRID 1060300
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HRID 1060300 반응식
Br[CH2:2][C:3]([C:5]1[C:13]2[S:12][C:11]([NH:14][C:15](=[O:17])[OH:16])=[N:10][C:9]=2[C:8]([O:18][CH3:19])=[CH:7][CH:6]=1)=O.[C:20]([O:24][C:25]([NH:27][C:28]([NH2:30])=[NH:29])=[O:26])([CH3:23])([CH3:22])[CH3:21]>C(#N)C>[C:20]([O:24][C:25]([NH:27][C:28]1[NH:29][CH:2]=[C:3]([C:5]2[C:13]3[S:12][C:11]([NH:14][C:15](=[O:17])[OH:16])=[N:10][C:9]=3[C:8]([O:18][CH3:19])=[CH:7][CH:6]=2)[N:30]=1)=[O:26])([CH3:23])([CH3:21])[CH3:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 22283192HCID 22283192, 화합물HCID 178454308HCID 178454308, 화합물

생성물 1

HCID 178488787HCID 178488787, 화합물수율 17%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

0.25 g of (7-bromoacetyl-4-methoxy-benzothiazol-2-yl)-carbamic acid methyll ester (0.0007 Mol) and 0.33 g of tert-butoxycarbonylguanidine (0.0021 Mol) were heated to reflux in acetonitril (3 ml) for 3 hrs. After evaporation of the solvent the residue was triturated with water (10 ml) and filtered. The filtrate was evaporated and the residue subjected to column chromatography (silicagel, ethyl-acetate/hexanes 1:1) to yield the title compound as a white solid (17%); F.p.: 255-265° C.

후처리

  1. customAfter evaporation of the solvent the residue
  2. customwas triturated with water (10 ml)
  3. filtrationfiltered
  4. customThe filtrate was evaporated

출처 및 근거

ORD 기록
ord-327fc0b09c3e426fad0a12e4d1a4817e
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06521754B2

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