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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Borane;tetrahydrofuran → HCID 58138929, 화합물

HRID 2061566
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HRID 2061566 반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[NH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([C:12]#[N:13])=[CH:7][C:6]=2[Br:14].O1CCCC1.B>C1COCC1>[F:16][C:2]([F:1])([F:15])[C:3]1[NH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([CH2:12][NH2:13])=[CH:7][C:6]=2[Br:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723981Borane;tetrahydrofuranHCID 58138925HCID 58138925, 화합물2회

생성물 1

HCID 58138929HCID 58138929, 화합물수율 113.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 2-(trifluoromethyl)-5-cyano-7-bromo-1H-indole (Intermediate 8; 200 mg, 0.692 mmol) in THF (10 mL) cooled in an ice-water bath was treated with borane tetrahydrofuran complex (1M in THF, 1.522 mL, 1.522 mmol) dropwise via a syringe and stirred under argon for 18 hrs while allowing to warm to room temp. The reaction mixture was then quenched with methanol (5 mL) and stirred at room temperature for 10 min. The reaction mixture was then evaporated to dryness to give the title compound as a white foam (230 mg), which was used in the next step without further purification;

후처리

  1. customThe reaction mixture was then quenched with methanol (5 mL)
  2. stirringstirred at room temperature for 10 min
  3. customThe reaction mixture was then evaporated to dryness

출처 및 근거

ORD 기록
ord-72fa84c93b0e4efd81edddfde4ab4e85
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08283365B2

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