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Triethylamine → HCID 21075718, 화합물

HRID 1373927
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HRID 1373927 반응식
[N:1]1([NH:7][C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[N:11]=[CH:10][C:9]=2[NH2:18])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.C(N(CC)CC)C.[CH2:26]([O:28][CH2:29][C:30](Cl)=[O:31])[CH3:27]>C(Cl)Cl.C(Cl)(Cl)Cl>[CH2:26]([O:28][CH2:29][C:30]([NH:18][C:9]1[CH:10]=[N:11][C:12]2[C:17]([C:8]=1[NH:7][N:1]1[CH2:2][CH2:3][O:4][CH2:5][CH2:6]1)=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:31])[CH3:27]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8471TriethylamineHCID 84189Ethoxyacetyl chlorideHCID 21075796HCID 21075796, 화합물

생성물 1

HCID 21075718HCID 21075718, 화합물수율 97.6%

시약·촉매·용매 2

HCID 6212Chloroform용매HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

A solution of N4-(morpholin-4-yl)quinoline-3,4-diamine (4.06 g, 16.6 mmol) in 50 mL of CH2Cl2 was treated with triethylamine (4.40 mL, 33.2 mmol) and cooled to 0° C. The solution was treated dropwise with ethoxyacetyl chloride (2.40 g, 17.4 mmol) and stirred under an atmosphere of nitrogen. The reaction mixture was allowed to slowly come to room temperature. After 2 d, the reaction mixture was concentrated under reduced pressure to yield a red semi-solid. The material was dissolved in CHCl3 and washed with water, 5% Na2CO3 solution and brine, dried over Na2SO4, filtered and dried to yield 2-ethoxy—N-{4-[(morpholin-4-yl)amino]quinolin-3-yl}acetamide (5.35 g) as a red/orange foam.

후처리

  1. customto slowly come to room temperature
  2. concentrationthe reaction mixture was concentrated under reduced pressure
  3. customto yield a red semi-solid
  4. washwashed with water, 5% Na2CO3 solution and brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. customdried

출처 및 근거

ORD 기록
ord-bef7b3cfaf914065a29683424e8ced7f
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07163947B2

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