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Tetrahydrofuran → HCID 18466606, 화합물

HRID 2229316
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HRID 2229316 반응식
Cl[C:2]1[C:7]([C:8]([NH:10][C:11]2[C:12]([NH:18][CH2:19][CH3:20])=[N:13][C:14]([F:17])=[CH:15][CH:16]=2)=[O:9])=[CH:6][C:5]([Br:21])=[CH:4][N:3]=1.C[Si]([N-][Si](C)(C)C)(C)C.[Na+].C1COCC1>N1C=CC=CC=1>[Br:21][C:5]1[CH:4]=[N:3][C:2]2[N:18]([CH2:19][CH3:20])[C:12]3[N:13]=[C:14]([F:17])[CH:15]=[CH:16][C:11]=3[NH:10][C:8](=[O:9])[C:7]=2[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 2724254Sodium bis(trimethylsilyl)amideHCID 184666372-Chloro-N-{2-(ethylarnino)-6-fluoro-3pyridinyl}-5-bromo-3-pyridinecarboxamide

생성물 1

HCID 18466606HCID 18466606, 화합물수율 69.5%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of the 2-chloro-N-{2-(ethylamino)-6-fluoro-3-pyridinyl}-5-bromo-3-pyridinecarboxamide (73.5 g, 216 mmol) in pyridine (435 mL) at 50° C. was added drop-wise a 1 M solution of NaHMDS in THF (520 mL, 520 mmol). After 10 min, the reaction was allowed to cool to room temperature, then poured over ice water (2 L). The resulting solid was filtered, rinse with water and then hexane. The solid was dried under reduced pressure to give the title compound (50.6 g, 69% yield) as a dark green solid.

후처리

  1. filtrationThe resulting solid was filtered
  2. washrinse with water
  3. customThe solid was dried under reduced pressure

출처 및 근거

ORD 기록
ord-32cb6215182042ba8a6c3b4b434417fe
출처 데이터셋
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06420359B1

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