1-Iodopentane → N,N-bis(pyridin-2-ylmethyl)pentan-1-amine

HRID 495261

반응식

HRID 495261 반응식
[OH-].[K+].[N:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][NH:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][N:13]=1.I[CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]>CN(C)C=O>[N:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][N:10]([CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][N:13]=1)[CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]

참가 물질

5

실험 절차

To 15 ml of N,N-dimethylformamide, 0.85 g potassium hydroxide, 1.0 g di(2-picolyl)amine, and 0.99 g 1-iodopentane were successively added. The mixture was stirred under nitrogen at 35 C for 2.5 hours before an additional 0.99 g 1-iodopentane were added. The mixture was then stirred for 16 hrs at 35 C under nitrogen. The reaction was quenched with 90 ml of water and extracted with two 50 ml portions of ethyl acetate. The combined organic layers were washed with two 25 ml portions of water, dried over anhydrous magnesium sulfate, and filtered. Following solvent removal, the orange oil obtained was purified by silica gel chromatography using a methanol/ethyl acetate mixed solvent system that was ramped from 0% to 10% methanol by volume during the course of the elution. An orange oil (0.98 g) was obtained.

후처리

  1. additionwere added
  2. customThe reaction was quenched with 90 ml of water
  3. extractionextracted with two 50 ml portions of ethyl acetate
  4. washThe combined organic layers were washed with two 25 ml portions of water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customFollowing solvent removal
  8. customthe orange oil obtained
  9. customwas purified by silica gel chromatography
  10. washwas ramped from 0% to 10% methanol by volume during the course of the elution

출처 및 근거

ORD 기록
ord-d41c0e4bf5f64009af1635b1389f2716
출처 데이터셋
uspto-grants-2009_05
특허 번호
US07538931B2

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