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p-Toluenesulfonic acid monohydrate → HCID 89704942, 화합물

HRID 528684
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반응식

HRID 528684 반응식
[C:1]([C@@H:3]1[CH2:7][CH2:6][CH2:5][N:4]1[C:8](=[O:26])[CH2:9][NH:10][C:11]([CH:13]1[CH2:18][CH2:17][N:16](C(OC(C)(C)C)=O)[CH2:15][CH2:14]1)=[O:12])#[N:2].O.CC1C=CC(S(O)(=O)=O)=CC=1>C(#N)C>[C:1]([C@@H:3]1[CH2:7][CH2:6][CH2:5][N:4]1[C:8](=[O:26])[CH2:9][NH:10][C:11]([CH:13]1[CH2:14][CH2:15][NH:16][CH2:17][CH2:18]1)=[O:12])#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 89705262HCID 89705262, 화합물

생성물 1

HCID 89704942HCID 89704942, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of (S)-tert-butyl 4-(2-(2-cyanopyrrolidine-1-yl)-2-oxoethylcarbamoyl)piperidine-1-carboxylate (0.100 g, 0.274 mmol) in 2 ml Acetonitrile was 4-methylbenzenesulfonic acid hydrate (0.073 g, 0.384 mmol) added and the mixture was stirred for 24 h. After evaporation of the volatiles, the sample was purified by preparative HPLC to yield an reddish oil.

후처리

  1. additionadded
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customAfter evaporation of the volatiles
  • customthe sample was purified by preparative HPLC
  • customto yield an reddish oil
  • 출처 및 근거

    ORD 기록
    ord-e033e2d277e044c783346e7bd90ac5db
    출처 데이터셋
    uspto-grants-2016_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09346814B2

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