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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Pyridine → HCID 21453097, 화합물

HRID 1283058
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HRID 1283058 반응식
N1C=CC=CC=1.[S:7]([NH:11][C:12]([NH2:14])=[O:13])([CH3:10])(=[O:9])=[O:8].[C:15](Cl)([Cl:17])=[O:16]>ClCCl>[S:7]([NH:11][C:12]([NH:14][C:15]([Cl:17])=[O:16])=[O:13])([CH3:10])(=[O:9])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 6371PhosgeneHCID 19365480Methanesulfonamide, N-(aminocarbonyl)-

생성물 1

HCID 21453097HCID 21453097, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

6.1 parts by volume of pyridine were added dropwise, while cooling, to a mixture of 10.5 parts by weight of N-mesylurea, 60 parts by volume of dichloromethane and 15.0 parts by weight of phosgene, while cooling, and after some hours at 0°C the excess of the phosgene was removed, the precipitate present was filtered off and the filtrate was completely concentrated in vacuo. A viscous oil remained, which had an absorption at 1800 cm-1 in the carbonyl region of the IR-spectrum. The substance was used without further purification for the production of the penicillin.

후처리

  1. temperaturewhile cooling
  2. customafter some hours at 0°C the excess of the phosgene was removed
  3. filtrationthe precipitate present was filtered off
  4. concentrationthe filtrate was completely concentrated in vacuo
  5. customan absorption at 1800 cm-1 in the carbonyl region of the IR-spectrum
  6. customThe substance was used without further purification for the production of the penicillin

출처 및 근거

ORD 기록
ord-fcd2681b9fb948d9bed487f4711edd62
출처 데이터셋
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03974142

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