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Triethylamine → 6-cyclopropyl-3-(2-morpholin-4-ylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione

HRID 1889329
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HRID 1889329 반응식
[NH2:1][C:2]1[S:3][C:4]([CH:11]2[CH2:13][CH2:12]2)=[CH:5][C:6]=1[C:7]([O:9]C)=O.Cl[C:15](Cl)([O:17]C(=O)OC(Cl)(Cl)Cl)Cl.C(N(CC)CC)C.[N:33]1([CH2:39][CH2:40][NH2:41])[CH2:38][CH2:37][O:36][CH2:35][CH2:34]1>C(Cl)Cl>[CH:11]1([C:4]2[S:3][C:2]3[NH:1][C:15](=[O:17])[N:41]([CH2:40][CH2:39][N:33]4[CH2:38][CH2:37][O:36][CH2:35][CH2:34]4)[C:7](=[O:9])[C:6]=3[CH:5]=2)[CH2:13][CH2:12]1
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참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 94429TriphosgeneHCID 4082852-MorpholinoethylamineHCID 45089420Methyl 2-amino-5-cyclopropylthiophene-3-carboxylate

생성물 1

HCID 593518146-cyclopropyl-3-(2-morpholin-4-ylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione수율 93.3%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To a solution (15 mL) of methyl 2-amino-5-cyclopropylthiophene-3-carboxylate (0.5 g) in methylene chloride were added triphosgene (0.98 g) and triethylamine (1.7 mL), and the mixture was stirred at room temperature for 2 hr. To the reaction mixture was added 2-morpholin-4-ylethanamine (0.99 g), and the mixture was further stirred at room temperature for 1 hr. The reaction mixture was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in methanol (10 mL), sodium methoxide (0.5 g) was added, and the mixture was stirred at 60° C. for 2 hr. The reaction mixture was neutralized with hydrochloric acid (10% methanol solution), insoluble material was filtered off, and the solvent was evaporated under reduced pressure. The precipitated solid was collected by filtration to give the title compound as a colorless solid (0.76 g, 84%).

후처리

  1. stirringthe mixture was further stirred at room temperature for 1 hr
  2. washThe reaction mixture was washed with water and saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure
  5. dissolutionThe obtained residue was dissolved in methanol (10 mL)
  6. additionsodium methoxide (0.5 g) was added
  7. stirringthe mixture was stirred at 60° C. for 2 hr
  8. filtrationwas filtered off
  9. customthe solvent was evaporated under reduced pressure
  10. filtrationThe precipitated solid was collected by filtration

출처 및 근거

ORD 기록
ord-f5cddf6eb5a8456fa834712d35be64ad
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501750B2

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