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Triethylamine → Sch 28080

HRID 544447
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HRID 544447 반응식
Cl[CH:2]([C:6](=O)[CH3:7])[CH2:3][C:4]#[N:5].[NH2:9][C:10]1[C:15]([O:16][CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:14][CH:13]=[CH:12][N:11]=1.C(N(CC)CC)C>C(O)C>[CH2:17]([O:16][C:15]1[C:10]2[N:11]([C:2]([CH2:3][C:4]#[N:5])=[C:6]([CH3:7])[N:9]=2)[CH:12]=[CH:13][CH:14]=1)[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 903342-Amino-3-benzyloxypyridineHCID 139002363-Chloro-4-oxopentanenitrile

생성물 1

HCID 108137Sch 28080

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 0.86 g. of 3-chloro-4-oxopentanonitrile, 0.92 g. of 2-amino-3-phenylmethoxypyridine and 0.5 ml. of triethylamine in 15 ml. of ethanol was stirred for 16 hours, then concentrated to remove the triethylamine and ethanol. The residue was dissolved in methylene chlorideand washed with water. The methylene chloride was concentrated and the residual oil was dissolved in 20 ml. of boiling acetonitrile, filtered, cooled, and treated with hydrogen chloride/methanol with cooling to give 0.22 g. of the desired product (m.p. 163°-166° C.).

후처리

  1. concentrationconcentrated
  2. customto remove the triethylamine and ethanol
  3. dissolutionThe residue was dissolved in methylene
  4. washchlorideand washed with water
  5. concentrationThe methylene chloride was concentrated
  6. dissolutionthe residual oil was dissolved in 20 ml
  7. filtrationof boiling acetonitrile, filtered
  8. temperaturecooled
  9. additiontreated with hydrogen chloride/methanol
  10. temperaturewith cooling
  11. customto give 0.22 g

출처 및 근거

ORD 기록
ord-cda23162da864db180393d4694b21bf1
출처 데이터셋
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04450164

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