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Triethylamine → 1-(2-(4-(5-(Morpholinosulfonyl)thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one

HRID 507551
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HRID 507551 반응식
CS([C:5]1[N:10]=[C:9]([C:11]2[S:12][C:13]([S:16]([N:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)(=[O:18])=[O:17])=[CH:14][CH:15]=2)[CH:8]=[CH:7][N:6]=1)(=O)=O.[NH2:25][CH2:26][CH2:27][N:28]1[CH2:32][CH2:31][NH:30][C:29]1=[O:33].C(N(CC)CC)C>C1(C)C=CC=CC=1>[O:22]1[CH2:23][CH2:24][N:19]([S:16]([C:13]2[S:12][C:11]([C:9]3[CH:8]=[CH:7][N:6]=[C:5]([NH:25][CH2:26][CH2:27][N:28]4[CH2:32][CH2:31][NH:30][C:29]4=[O:33])[N:10]=3)=[CH:15][CH:14]=2)(=[O:18])=[O:17])[CH2:20][CH2:21]1
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 80480N-(2-Aminoethyl)ethyleneureaHCID 602043782-(Methylsulfonyl)-4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidine

생성물 1

HCID 602043771-(2-(4-(5-(Morpholinosulfonyl)thiophen-2-yl)pyrimidin-2-ylamino)ethyl)imidazolidin-2-one

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of 2-(methylsulfonyl)-4-(5-(morpholinosulfonyl)thiophen-2-yl)pyrimidine (100 mg, 0.26 mmol), 1-(2-aminoethyl)imidazolidin-2-one (36 mg, 0.28 mmol) and triethylamine (56 mg, 0.52 mmol) in toluene (3 mL) was refluxed for 6 h. After cooling to rt, the solvent was evaporated in vacuo and then methanol (5 mL) was added. After stirring for 15 min the solid was filtered and dried to give the title compound with a light yellow color (81 mg, 72%). MS (M+H)+ 439.

후처리

  1. temperaturewas refluxed for 6 h
  2. customthe solvent was evaporated in vacuo
  3. additionmethanol (5 mL) was added
  4. filtrationwas filtered
  5. customdried

출처 및 근거

ORD 기록
ord-53cfaab6984e42dbbd51ca1cde4f7407
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07786132B2

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