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Piperidine-1-carboxamidine → HCID 178447459, 화합물

HRID 1399762
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HRID 1399762 반응식
[N:1]1([C:7](=[NH:9])[NH2:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:10]([C:25](OCC)=[O:26])([C:20](OCC)=[O:21])[CH:11]([C:15]([O:17]CC)=[O:16])[CH2:12][CH2:13][CH3:14].C[O-].[Na+]>CO>[OH:21][C:20]1[C:10]([CH:11]([CH2:12][CH2:13][CH3:14])[C:15]([OH:17])=[O:16])=[C:25]([OH:26])[N:8]=[C:7]([N:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)[N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 205051Piperidine-1-carboxamidineHCID 10942334Sodium MethoxideHCID 12679371Triethyl pentane-1,1,2-tricarboxylate

생성물 1

HCID 178447459HCID 178447459, 화합물

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a solution of piperidine-1-carboximidamide (dimer complexated with H2SO4) (1.32 g; 10.4 mmol) and triethyl pentane-1,1,2-tricarboxylate (3 g; 10.4 mmol) in methanol (15 mL) was slowly added a solution of sodium methoxide in methanol (25% w:w) (4.76 mL; 20.81 mmol) and the reaction was heated to reflux for 18 h. The volatiles were removed under reduced pressure and the crude residue was used as such in the next reaction.

후처리

  1. temperaturethe reaction was heated
  2. temperatureto reflux for 18 h
  3. customThe volatiles were removed under reduced pressure
  4. customsuch in the next reaction

출처 및 근거

ORD 기록
ord-d2d9743fab92481b8fb9d3b09950e8be
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08906906B2

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