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Triethylamine → HCID 59389328, 화합물

HRID 2357924
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HRID 2357924 반응식
C(N(CC)CC)C.[OH:8][CH:9]([C:11]1[CH:29]=[C:14]2[C:15]([C:21]3[CH:22]([CH3:28])[CH2:23][C:24](=[O:27])[NH:25][N:26]=3)=[CH:16][CH:17]=[C:18]([O:19][CH3:20])[N:13]2[N:12]=1)[CH3:10]>CS(C)=O>[C:9]([C:11]1[CH:29]=[C:14]2[C:15]([C:21]3[CH:22]([CH3:28])[CH2:23][C:24](=[O:27])[NH:25][N:26]=3)=[CH:16][CH:17]=[C:18]([O:19][CH3:20])[N:13]2[N:12]=1)(=[O:8])[CH3:10]
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참가 물질

4

반응물 2

HCID 8471TriethylamineHCID 59389404HCID 59389404, 화합물

생성물 1

HCID 59389328HCID 59389328, 화합물수율 59.8%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

Triethylamine (1.46 mL) was added to a solution of the compound of Example 238 (315 mg) in DMSO (10 mL). While the mixture was stirred at room temperature, sulfur trioxide-pyridine complex (829 mg) was added at once and the mixture was further stirred at room temperature for 1 hour. Subsequently, the reaction was quenched by adding water (100 mL). Filtration of the resulting crystals afforded the title compound as a colorless powder (187 mg).

후처리

  1. additionsulfur trioxide-pyridine complex (829 mg) was added at once and the mixture
  2. stirringwas further stirred at room temperature for 1 hour
  3. customSubsequently, the reaction was quenched
  4. additionby adding water (100 mL)
  5. filtrationFiltration of the resulting crystals

출처 및 근거

ORD 기록
ord-15c21e2c88c84b3ba31a669aaffd280b
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07763617B2

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