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Dimethylamine → 2-amino-N,N-dimethylpyridine-4-carboxamide

HRID 1446702
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HRID 1446702 반응식
[Li+].C[CH:3]([N-:5][CH:6](C)C)C.CNC.C[O:13][C:14]([C:16]1[CH:21]=[CH:20][N:19]=[C:18]([NH2:22])[CH:17]=1)=O>>[NH2:22][C:18]1[CH:17]=[C:16]([CH:21]=[CH:20][N:19]=1)[C:14]([N:5]([CH3:6])[CH3:3])=[O:13]
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참가 물질

4

반응물 3

HCID 674DimethylamineHCID 236984Methyl 2-aminopyridine-4-carboxylateHCID 2724682Lithium diisopropylamide

생성물 1

HCID 621546592-amino-N,N-dimethylpyridine-4-carboxamide

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온도
85 °C

실험 절차

To LDA (7.3 mL, 13 mmol, 1.8M in ether/heptane) at 0° C., add dropwise dimethylamine (13 mL, 26 mmol, 2M in THF) under nitrogen. Stir for 30 minutes and add 2-amino-4-pyridine carboxylic acid methyl ester (2 g, 13 mmol, in 3 mL of anhydrous THF and 2 mL of anhydrous ether). Seal and heat at 85° C. overnight. Cool the mixture to room temperature and quench with water. Dilute with EtOAc and isolate the top organic layer. Extract the aqueous layer further with saturated sodium bicarbonate and ether, then DCM. Pool all the organic layers, dry (MgSO4) and concentrate. Purify by strong cation exchange (SCX) column to obtain the crude product and use in the next step without further purification. LCMS (ES), m/z 166 (M+1).

후처리

  1. customSeal
  2. temperatureCool the mixture to room temperature
  3. customquench with water
  4. additionDilute with EtOAc
  5. customisolate the top organic layer
  6. extractionExtract the aqueous layer further with saturated sodium bicarbonate and ether
  7. dry with materialPool all the organic layers, dry (MgSO4)
  8. concentrationconcentrate
  9. customPurify by strong cation exchange (SCX) column

출처 및 근거

ORD 기록
ord-162ab913f343489eadaed34439dda914
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07666879B2

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