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Triethylamine → (S)-tert-butyl 3-((7-chloro-3-cyanoisoquinolin-1-yl)amino)pyrrolidine-1-carboxylate

HRID 1476892
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HRID 1476892 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Cl:12])[CH:10]=2)[CH:5]=[C:4]([C:13]#[N:14])[N:3]=1.[NH2:15][C@H:16]1[CH2:20][CH2:19][N:18]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:17]1.CCN(CC)CC>CN1C(=O)CCC1>[Cl:12][C:9]1[CH:10]=[C:11]2[C:6]([CH:5]=[C:4]([C:13]#[N:14])[N:3]=[C:2]2[NH:15][C@H:16]2[CH2:20][CH2:19][N:18]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:17]2)=[CH:7][CH:8]=1
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5

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HCID 8471TriethylamineHCID 854071tert-butyl (3S)-3-aminopyrrolidine-1-carboxylateHCID 846880831,7-Dichloroisoquinoline-3-carbonitrile

생성물 1

HCID 90386864(S)-tert-butyl 3-((7-chloro-3-cyanoisoquinolin-1-yl)amino)pyrrolidine-1-carboxylate수율 79%

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매

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온도
160 °C

실험 절차

To a solution of 1,7-dichloroisoquinoline-3-carbonitrile (500 mg, 2.24 mmol) in NMP (5 mL) was added (S)-tert-butyl 3-aminopyrrolidine-1-carboxylate (460 mg, 2.46 mmol) and Et3N (453 mg, 4.48 mmol). The solution was heated to 160° C. for 30 minutes in a microwave reactor. The reaction was quenched with H2O (20 mL) and extracted with EtOAc (3×10 mL). The organic layers were combined and concentrated in vacuo. The crude product was purified by column chromatography eluting with ethyl acetate and petroleum ether (EtOAc/PE=1:10 to 1:5 gradient) to give the title compound (660 mg, 79%). ESI-MS m/z [M+H-tert-butyl]+ 317.

후처리

  1. customThe reaction was quenched with H2O (20 mL)
  2. extractionextracted with EtOAc (3×10 mL)
  3. concentrationconcentrated in vacuo
  4. customThe crude product was purified by column chromatography
  5. washeluting with ethyl acetate and petroleum ether (EtOAc/PE=1:10 to 1:5 gradient)

출처 및 근거

ORD 기록
ord-e9e52bcb4d5d4d8cb8e3ce8de20c3c18
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09402841B2

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