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Triethylamine → HCID 23020436, 화합물

HRID 747178
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HRID 747178 반응식
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[O:9][CH:10]=[CH:11][CH:12]=2)[C:5]([C:13]2[CH:18]=[CH:17][N:16]([CH2:19][C:20]([OH:22])=O)[C:15](=[O:23])[CH:14]=2)=[CH:4][N:3]=1.ON1C2C=CC=CC=2N=N1.CN(C)CCCN=C=NCC.Cl.[CH2:46]([NH:48][CH2:49][CH3:50])[CH3:47].C(N(CC)CC)C>CN(C)C=O.O>[CH2:46]([N:48]([CH2:49][CH3:50])[C:20](=[O:22])[CH2:19][N:16]1[CH:17]=[CH:18][C:13]([C:5]2[C:6]([C:8]3[O:9][CH:10]=[CH:11][CH:12]=3)=[N:7][C:2]([NH2:1])=[N:3][CH:4]=2)=[CH:14][C:15]1=[O:23])[CH3:47]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 8471TriethylamineHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 10197650Diethylammonium chlorideHCID 59749123HCID 59749123, 화합물

생성물 1

HCID 23020436HCID 23020436, 화합물수율 6.2%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

실험 절차

A suspension of {4-[2-amino-4-(2-furyl)-5-pyrimidinyl]-2-oxo-1,2-dihydro-1-pyridinyl}acetic acid (10 mg, 32 μmol), 1-hydroxybenzotriazole (15 mg, 98 μmol), 3-(3′-dimethylaminopropyl)-1-ethylcarbodiimide (15 mg, 96 μmol), diethylamine hydrochloride (18 mg, 164 μmol) and triethylamine (22 μl, 160 μmol) in N,N-dimethylformamide (1.0 ml) was stirred at room temperature for 17 hours. The reaction mixture was diluted with water and then extracted with ethyl acetate. The organic layer was concentrated and then purified by HPLC, to give the title compound (0.73 mg, 6%).

후처리

  1. extractionextracted with ethyl acetate
  2. concentrationThe organic layer was concentrated
  3. custompurified by HPLC

출처 및 근거

ORD 기록
ord-1da8b26b29dd4a90a75b56ffddfba487
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07396836B2

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