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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl (2-methyl-3-hydroxy-4-hydroxymethyl-5-pyridylmethyl)malonate → HCID 9813750, 화합물

HRID 2117254
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HRID 2117254 반응식
C([O:3][C:4](=[O:22])[CH:5]([CH2:11][C:12]1[C:13]([CH2:20][OH:21])=[C:14]([OH:19])[C:15]([CH3:18])=[N:16][CH:17]=1)[C:6]([O:8]CC)=[O:7])C>[OH-].[Na+].C(O)C>[CH3:18][C:15]1[C:14]([OH:19])=[C:13]([CH2:20][OH:21])[C:12]([CH2:11][CH:5]([C:6]([OH:8])=[O:7])[C:4]([OH:22])=[O:3])=[CH:17][N:16]=1
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참가 물질

4

반응물 1

HCID 9966477Diethyl (2-methyl-3-hydroxy-4-hydroxymethyl-5-pyridylmethyl)malonate

생성물 1

HCID 9813750HCID 9813750, 화합물

시약·촉매·용매 2

HCID 702Ethanol용매HCID 14798Sodium Hydroxide용매

실험 절차

The product of Example 25, of structure XXIX (620 mg, 2.0 mmol) was dissolved in aqueous NaOH (2 M, 4 mL) and stirred at room temperature for 1 hour. The reaction was quenched by adding 6 N HCl to give pH 4 to 5. The solution was diluted with 95% ethanol, separated from the precipitated salts and evaporated to give 540 mg.

후처리

  1. customThe reaction was quenched
  2. additionby adding 6 N HCl
  3. customto give pH 4 to 5
  4. customseparated from the precipitated salts
  5. customevaporated
  6. customto give 540 mg

출처 및 근거

ORD 기록
ord-9a4e806a99194468a37edcb6e7fd43aa
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07442689B2

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