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Trimethylphosphine → HCID 58565367, 화합물

HRID 2175329
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HRID 2175329 반응식
[N:1]([CH:4]([C:6]1[N:7]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([F:21])[CH:16]=2)[C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH3:5])=[N+]=[N-].CP(C)C>O1CCCC1>[F:21][C:17]1[CH:16]=[C:15]([N:7]2[C:8]3[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=3)[CH:14]=[C:6]2[CH:4]([NH2:1])[CH3:5])[CH:20]=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 68983TrimethylphosphineHCID 58565371HCID 58565371, 화합물

생성물 1

HCID 58565367HCID 58565367, 화합물수율 133.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of 2-(1-azidoethyl)-1-(3-fluorophenyl)-1H-indole (0.14 g, 0.50 mmol) in tetrahydrofuran (3 mL) was added 1.00 M trimethylphosphine in tetrahydrofuran (0.75 mL, 0.75 mmol). The mixture was stirred at room temperature for 1 hour. The mixture was concentrated to give crude product (0.17 g), which was used directly in the next step. LCMS calculated for C16H13FN(M-NH2)+: m/z=238.1. Found: 238.1.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. concentrationThe mixture was concentrated

출처 및 근거

ORD 기록
ord-3735d0eee7ad43c4aac3b20a7631e380
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062055B2

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