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Hydrazine → (S)-1-(5-(4-chlorophenyl)oxazol-2-yl)ethanamine

HRID 57388
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HRID 57388 반응식
NN.[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[O:14][C:13]([C@@H:15]([N:17]3C(=O)C4C(=CC=CC=4)C3=O)[CH3:16])=[N:12][CH:11]=2)=[CH:6][CH:5]=1>C(O)C>[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([C:10]2[O:14][C:13]([C@@H:15]([NH2:17])[CH3:16])=[N:12][CH:11]=2)=[CH:8][CH:9]=1
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참가 물질

4

반응물 2

HCID 9321HydrazineHCID 90414733(S)-2-(1-(5-(4-chlorophenyl)oxazol-2-yl)ethyl)isoindoline-1,3-dione

생성물 1

HCID 42048108(S)-1-(5-(4-chlorophenyl)oxazol-2-yl)ethanamine수율 73.7%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
80 °C

실험 절차

Hydrazine (0.55 ml, 6.09 mmol) was added to a solution of (S)-2-(1-(5-(4-chlorophenyl)oxazol-2-yl)ethyl)isoindoline-1,3-dione (430 mg, 1.219 mmol) in ethanol (15 ml) and heated at 80° C. for 13 hours. The reaction was concentrated in vacuo. Flash column chromatography (silica, 40 g) eluting with 2-10% MeOH/DCM afforded the desired product (200 mg, yellow oil). 1H NMR (400 MHz, CDCl3) δ 7.67-7.51 (m, 9H), 7.47-7.35 (m, 8H), 7.31-7.21 (m, 1H), 4.25 (q, J=6.8 Hz, 4H), 1.97-1.66 (m, 15H), 1.63-1.48 (m, 2H). HRMS(B) tR=1.49 min; MS m/z 222.0560

후처리

  1. concentrationThe reaction was concentrated in vacuo
  2. washFlash column chromatography (silica, 40 g) eluting with 2-10% MeOH/DCM

출처 및 근거

ORD 기록
ord-e945619f346d4e7185708695a18d7d11
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434719B2

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