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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 86644292, 화합물 → HCID 25147517, 화합물

HRID 1807438
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HRID 1807438 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([S:9]([N:12]([CH2:28][P:29](=[O:36])([O:33]CC)[O:30]CC)[C:13]2[CH:14]=[C:15]3[C:19](=[CH:20][CH:21]=2)[N:18]([C:22]2[N:27]=[CH:26][CH:25]=[CH:24][N:23]=2)[CH2:17][CH2:16]3)(=[O:11])=[O:10])[CH:5]=[C:6]([Cl:8])[CH:7]=1>ClCCl.CO>[Cl:1][C:2]1[CH:3]=[C:4]([S:9]([N:12]([CH2:28][P:29](=[O:30])([OH:33])[OH:36])[C:13]2[CH:14]=[C:15]3[C:19](=[CH:20][CH:21]=2)[N:18]([C:22]2[N:23]=[CH:24][CH:25]=[CH:26][N:27]=2)[CH2:17][CH2:16]3)(=[O:10])=[O:11])[CH:5]=[C:6]([Cl:8])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86644292HCID 86644292, 화합물

생성물 1

HCID 25147517HCID 25147517, 화합물

시약·촉매·용매 2

HCID 887Methanol용매2회HCID 6344Dichloromethane용매

실험 절차

70 mg diethyl {[(3,5-dichloro-phenylsulphonyl)-(1-pyrimidin-2-yl-2,3-dihydro-1H-indol-5-yl)-amino]-methyl}-phosphonate are dissolved in 3 ml dichloromethane. Under argon 200 μl trimethylsilylbromide are added thereto and the mixture is refluxed for 2 hours. After cooling to ambient temperature 1 ml of methanol is added and the mixture is stirred for a further 1 hour. Then the solvents are eliminated in vacuo. The residue is taken up in 3 ml of methanol, stirred for 10 minutes and the solvent is eliminated in vacuo. The residue thus obtained is extracted from dichloromethane with 1% methanol. The solid is suction filtered and dried.

후처리

  1. additionUnder argon 200 μl trimethylsilylbromide are added
  2. temperaturethe mixture is refluxed for 2 hours
  3. additionis added
  4. stirringstirred for 10 minutes
  5. customThe residue thus obtained
  6. extractionis extracted from dichloromethane with 1% methanol
  7. filtrationfiltered
  8. customdried

출처 및 근거

ORD 기록
ord-ab12f9d3f16a441f9875449ca4a379c1
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08357689B2

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