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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Spiro[chromene-2,3'-pyrrolidine] hydrochloride → 1047656-03-0

HRID 2036100
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HRID 2036100 반응식
[ClH:1].[NH:2]1[CH2:6][CH2:5][C:4]2([CH:15]=[CH:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[O:7]2)[CH2:3]1>CO.[C].[Pd]>[ClH:1].[NH:2]1[CH2:6][CH2:5][C:4]2([CH2:15][CH2:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[O:7]2)[CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68552129Spiro[chromene-2,3'-pyrrolidine] hydrochloride

생성물 1

HCID 685550421047656-03-0수율 86%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 887Methanol용매

실험 절차

Spiro[chromene-2,3′-pyrrolidine] hydrochloride (150 mg) synthesized in Example 33(1) and 5% palladium-carbon (30 mg) were suspended in methanol (10 mL), and the suspension was stirred overnight under a hydrogen atmosphere at room temperature. The catalyst was removed by filtration through celite, and the solvent was evaporated under reduced pressure to give the object product (130 mg, 86%).

후처리

  1. customThe catalyst was removed by filtration through celite
  2. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-d62175440f334cfb87d01dd88cc4f2aa
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08575167B2

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