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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-Butyl ((3-oxoisoindolin-5-yl)methyl)carbamate → 6-(Aminomethyl)-2,3-dihydro-1H-isoindol-1-one

HRID 410488
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HRID 410488 반응식
C(OC(=O)[NH:7][CH2:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[CH2:14][NH:13][C:12]2=[O:18])(C)(C)C>Cl>[NH2:7][CH2:8][C:9]1[CH:10]=[C:11]2[C:15]([CH2:14][NH:13][C:12]2=[O:18])=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 67259861tert-Butyl ((3-oxoisoindolin-5-yl)methyl)carbamate

생성물 1

HCID 584561586-(Aminomethyl)-2,3-dihydro-1H-isoindol-1-one수율 92.5%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A mixture of the product of Step 2 (100 g, 0.38 mol) and HCl (dissolved in MeOH, 3 M, 500 ml) was stirred overnight. Removal of the solvent gave a solid which was washed with Et2O and dried to afford 6-(aminomethyl)-2,3-dihydro-1H-isoindol-1-one (57 g, 76% yield). 1H-NMR (300 MHz, D2O) δ: 7.69-7.67 (m, 1H), 7.52 (s, 1H), 7.45-7.43 (m, 1H), 4.39 (s, 2H), 4.17 (s, 2H).

후처리

  1. customRemoval of the solvent
  2. customgave a solid which
  3. washwas washed with Et2O
  4. customdried

출처 및 근거

ORD 기록
ord-52fe6ca7f23e43cb82927a0f075f8f81
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08759366B2

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