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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-Butyl (3S)-3-(4-quinolylamino)pyrrolidine-1-carboxylate → N-[(3S)-Pyrrolidin-3-yl]quinolin-4-amine

HRID 333939
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인쇄 미리보기

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HRID 333939 반응식
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([NH:11][C@H:12]2[CH2:16][CH2:15][N:14](C(OC(C)(C)C)=O)[CH2:13]2)=[CH:3][CH:2]=1>ClCCl.FC(F)(F)C(O)=O>[NH:14]1[CH2:15][CH2:16][C@H:12]([NH:11][C:4]2[C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[N:1]=[CH:2][CH:3]=2)[CH2:13]1
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참가 물질

4

반응물 1

HCID 86691593tert-Butyl (3S)-3-(4-quinolylamino)pyrrolidine-1-carboxylate

생성물 1

HCID 66835796N-[(3S)-Pyrrolidin-3-yl]quinolin-4-amine

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 6422Trifluoroacetic acid용매

실험 절차

tert-Butyl (3S)-3-(4-quinolylamino)pyrrolidine-1-carboxylate (231 mg, 0.68 mmol) was dissolved in a 1:1 mixture of dichloromethane and trifluoroacetic acid (2 ml) and stirred at room temperature for 15 minutes. The mixture was evaporated to dryness under reduced pressure and the residue obtained was used directly in the next step.

후처리

  1. customThe mixture was evaporated to dryness under reduced pressure
  2. customthe residue obtained

출처 및 근거

ORD 기록
ord-2df75cc88bef4c0092b546ebb476418e
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08883791B2

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