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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Formaldehyde → Ethyl 2-(6-(dimethylamino)pyridin-2-yl)acetate

HRID 572918
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HRID 572918 반응식
N[C:2]1[N:7]=[C:6]([CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH:5]=[CH:4][CH:3]=1.[CH2:14]=O.[BH3-][C:17]#[N:18].[Na+]>CO.CC(O)=O>[CH3:14][N:18]([CH3:17])[C:2]1[N:7]=[C:6]([CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH:5]=[CH:4][CH:3]=1
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참가 물질

6

반응물 3

HCID 712FormaldehydeHCID 5003444Sodium cyanoborohydrideHCID 13060163Ethyl (6-aminopyridin-2-yl)acetate

생성물 1

HCID 86719100Ethyl 2-(6-(dimethylamino)pyridin-2-yl)acetate수율 57.9%

시약·촉매·용매 2

HCID 176Acetic Acid촉매HCID 887Methanol용매

실험 절차

To the solution of ethyl 2-(6-aminopyridin-2-yl)acetate (150 mg, 0.83 mmol) and paraformaldehyde (54.8 mg, 1.83 mmol) in methanol (6 mL) was added NaBH3CN (130.3 mg, 2.08 mmol) and AcOH (1 drop, cat.). The mixture was stirred at room temperature for 12 h. Then, the reaction was quenched with aqueous ammonium chloride and extracted with DCM. The organic layer was with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by a standard method to get desired product (100 mg).

후처리

  1. customThen, the reaction was quenched with aqueous ammonium chloride
  2. extractionextracted with DCM
  3. dry with materialdried over sodium sulfate
  4. customevaporated under reduced pressure
  5. customThe residue was purified by a standard method

출처 및 근거

ORD 기록
ord-58578459920b401ea0f1152885408c78
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09029531B2

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