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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 178488665, 화합물

HRID 714446
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인쇄 미리보기

반응식

HRID 714446 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:14]([C:15]#[N:16])=[CH:13][N:12]=[C:11]([S:17]C3C=CC=CC=3)[C:10]=2[C:24]#[N:25])=[CH:5][CH:4]=1.[S-2].[Na+].[Na+].Cl>CN(C=O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[C:14]([C:15]#[N:16])=[CH:13][N:12]=[C:11]([SH:17])[C:10]=2[C:24]#[N:25])=[CH:7][CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14804Sodium SulfideHCID 66631772HCID 66631772, 화합물

생성물 1

HCID 178488665HCID 178488665, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

1.3 g (3.028 mmol) of 4-(4-methoxyphenyl)-2-(phenylsulfanyl)pyridine-3,5-dicarbonitrile (Example 48A) were initially charged in 11 ml of DMF. 284 mg (3.634 mmol) of sodium sulfide were added, and the mixture was then stirred at 80° C. for 2 h and stirred further at RT overnight. 6 ml of 1N hydrochloric acid were added to the reaction mixture, and the reaction solution was evaporated. The residue was purified by preparative HPLC (Chromasil, water/acetonitrile).

후처리

  1. stirringstirred further at RT overnight
  2. customthe reaction solution was evaporated
  3. customThe residue was purified by preparative HPLC (Chromasil, water/acetonitrile)

출처 및 근거

ORD 기록
ord-4b8871a984c541ea8019f554327ee229
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187428B2

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