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Triphenylphosphine → 2-((R)-1-chloro-ethyl)-isonicotinonitrile

HRID 1694556
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인쇄 미리보기

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HRID 1694556 반응식
O[C@H:2]([C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][N:11]=1)[C:7]#[N:8])[CH3:3].C1C(=O)N([Cl:19])C(=O)C1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>>[Cl:19][C@@H:2]([C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][N:11]=1)[C:7]#[N:8])[CH3:3]
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참가 물질

4

반응물 3

HCID 11776Triphenylphosphine2회HCID 31398Chlorosuccinimide2회HCID 598688242-((S)-1-Hydroxy-ethyl)-isonicotinonitrile

생성물 1

HCID 598688402-((R)-1-chloro-ethyl)-isonicotinonitrile수율 7%

반응 조건

온도
30 °C

실험 절차

The title compound was prepared from 2-((S)-1-hydroxy-ethyl)-isonicotinonitrile (620 mg, 4.18 mmol) according to General Method C, except that 1.0 equiv. NCS and 1.0 equiv. PPh3 were used. After 24 hrs reaction time another 0.2 equiv. each of NCS and PPh3 were added and the temperature was increased to 30° C. for 12 h. Workup and purification by flash column chromatography yielded the title compound (46 mg, 7% yield) with 82% ee. 1H NMR (CDCl3) δ 8.74 (d, 1H), 7.76 (s, 1H), 7.46 (dd, 1H), 5.16 (q, 1H), 1.88 (d, 3H).

후처리

  1. additionwere added
  2. customWorkup and purification by flash column chromatography

출처 및 근거

ORD 기록
ord-f4229fa516fb4b7c9afb5967157b7b19
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158785B2

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