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Cyclopentylamine → HCID 10243173, 화합물

HRID 1642727
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HRID 1642727 반응식
Cl[CH2:2][C:3]([N:5]1[C@@H:9]([CH3:10])[CH2:8][CH2:7][C@H:6]1[C:11]#[N:12])=[O:4].[CH:13]1([NH2:18])[CH2:17][CH2:16][CH2:15][CH2:14]1>C(#N)C>[CH:13]1([NH:18][CH2:2][C:3]([N:5]2[C@@H:9]([CH3:10])[CH2:8][CH2:7][C@H:6]2[C:11]#[N:12])=[O:4])[CH2:17][CH2:16][CH2:15][CH2:14]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2906CyclopentylamineHCID 16090846(2S,5S)-1-(Chloroacetyl)-5-methylpyrrolidine-2-carbonitrile

생성물 1

HCID 10243173HCID 10243173, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

(2S,5S)-1-(2-Chloro-acetyl)-5-methyl-pyrrolidine-2-carbonitrile (50 mg, 0.30 mmol) and cyclopentylamine (0.059 mL, 0.6 mmol) were dissolved in acetonitrile (2 mL) and stirred overnight. The product was purified by reverse phase HPLC eluting with 0% to 70% acetonitrile/0.1% aqueous trifluoroacetic acid. 1H NMR (300 MHz, methanol-d4) δ ppm 1.36 (d, J=6.44 Hz, 3H), 1.68 (m, 5H), 1.85 (m, 3H), 2.16 (m, 3H), 2.38 (m, 3H), 3.60 (m, 1H), 4.20 (m, 1H), 4.77 (m, 1H). MS (ESI) m/z 236 (M+H)+.

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  1. customThe product was purified by reverse phase HPLC
  2. washeluting with 0% to 70% acetonitrile/0.1% aqueous trifluoroacetic acid

출처 및 근거

ORD 기록
ord-cc60cece949547c9a19bef6dc60537af
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08119664B2

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