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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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benzyl 1-ethyl-1H-spiro[chromeno[4,3-c]pyrazole-4,4'-piperidine]-1'-carboxylate → 1-ethyl-1H-spiro[chromeno[4,3-c]pyrazole-4,4'-piperidine]

HRID 2204113
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인쇄 미리보기

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HRID 2204113 반응식
[CH2:1]([N:3]1[C:7]2[C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:13]=3[O:14][C:15]3([CH2:20][CH2:19][N:18](C(OCC4C=CC=CC=4)=O)[CH2:17][CH2:16]3)[C:6]=2[CH:5]=[N:4]1)[CH3:2].[H][H]>CO.[Pd]>[CH2:1]([N:3]1[C:7]2[C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:13]=3[O:14][C:15]3([CH2:20][CH2:19][NH:18][CH2:17][CH2:16]3)[C:6]=2[CH:5]=[N:4]1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 58551072benzyl 1-ethyl-1H-spiro[chromeno[4,3-c]pyrazole-4,4'-piperidine]-1'-carboxylateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 585507281-ethyl-1H-spiro[chromeno[4,3-c]pyrazole-4,4'-piperidine]수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

Benzyl 1-ethyl-1H-spiro[chromeno[4,3-c]pyrazole-4,4′-piperidine]-1′-carboxylate (530 mg, 1.3 mmol) was stirred in methanol (9.5 mL) with Pd/C (70 mg, 0.070 mmol) under a balloon of hydrogen for 16 h. The reaction was filtered through a syringe filter and the solvent evaporated to give 1-ethyl-1H-spiro[chromeno[4,3-c]pyrazole-4,4′-piperidine] (350 mg, 99%). ESI-MS m/z calc. 269.2, found 270.5 (M+1)+; Retention time: 0.80 minutes (3 min run).

후처리

  1. filtrationThe reaction was filtered through a syringe
  2. filtrationfilter
  3. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-2aa1cafaf14042f39af06aec21535003
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09365588B2

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