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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(S)-Tert-butyl 3-(azidomethyl)piperidine-1-carboxylate → tert-Butyl (3R)-3-(aminomethyl)piperidine-1-carboxylate

HRID 1478605
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반응식

HRID 1478605 반응식
[N:1]([CH2:4][C@H:5]1[CH2:10][CH2:9][CH2:8][N:7]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:6]1)=[N+]=[N-]>CO.[Pd]>[NH2:1][CH2:4][C@H:5]1[CH2:10][CH2:9][CH2:8][N:7]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 10083012(S)-Tert-butyl 3-(azidomethyl)piperidine-1-carboxylate

생성물 1

HCID 1502023tert-Butyl (3R)-3-(aminomethyl)piperidine-1-carboxylate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

(S)-tert-butyl 3-(azidomethyl)piperidine-1-carboxylate (5.38 g, 22.40 mmol) was dissolved in MeOH (50 ml), and then Pd/C (5% mol) was added, followed by stirring at room temperature under H2 (gas) for 9 hours. After the completion of the reaction, the reaction mixture was filtered through celite, followed by filtration and concentration under reduced pressure, and then the next reaction was advanced without purification.

후처리

  1. customAfter the completion of the reaction
  2. filtrationthe reaction mixture was filtered through celite
  3. filtrationfollowed by filtration and concentration under reduced pressure
  4. customthe next reaction
  5. customwas advanced without purification

출처 및 근거

ORD 기록
ord-f6fc61fefd43412c92d12202819e8678
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09403831B2

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