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Phenethylamine → 2-[Benzyl(methyl)amino]isonicotinic acid

HRID 2223739
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인쇄 미리보기

반응식

HRID 2223739 반응식
Cl[C:2]1[CH:7]=[C:6]([C:8]([OH:10])=[O:9])[CH:5]=[CH:4][N:3]=1.[CH2:11](CN)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[CH2:20]([N:22](CC)CC)C>C(Cl)Cl>[CH2:11]([N:22]([CH3:20])[C:2]1[CH:7]=[C:6]([CH:5]=[CH:4][N:3]=1)[C:8]([OH:10])=[O:9])[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1001PhenethylamineHCID 8471TriethylamineHCID 2369852-Chloroisonicotinic acid

생성물 1

HCID 226433412-[Benzyl(methyl)amino]isonicotinic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
120 °C

실험 절차

A mixture of 2-chloro-pyridine-4-carboxylic acid (300 mg, 1.9 mmol), benzylmethylamine (230 mg, 1.9 mmol) and triethylamine (192 mg, 1.9 mmol) is heated at 120° C. for 12 h. The residue is dissolved in CH2Cl2 (30 mL) and extracted with 1M aqueous NaOH (3×5 mL). The aqueous layer is adjusted to pH 1-2 with 12N aqueous HCl and extracted with EtOAc (6×5 mL). The organic extracts are combined, dried (MgSO4), and evaporated to provide the title compound.

후처리

  1. extractionextracted with 1M aqueous NaOH (3×5 mL)
  2. extractionextracted with EtOAc (6×5 mL)
  3. dry with materialdried (MgSO4)
  4. customevaporated

출처 및 근거

ORD 기록
ord-3c9bf81f05054c0fa46e4fcd2ccec058
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07375227B2

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