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Water → HCID 70232275, 화합물

HRID 1977431
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HRID 1977431 반응식
[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][N:7]=[CH:8][C:9]=2[O:11][C:12]2[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][CH:13]=2)[S:4][C:3]=1[C:19]([NH2:21])=[O:20].C(N(CC)CC)C.O.[O:30]1CCC[CH2:31]1>>[Cl:18][C:15]1[CH:14]=[CH:13][C:12]([O:11][C:9]2[C:10]3[C:2]4[NH:1][C:31](=[O:30])[NH:21][C:19](=[O:20])[C:3]=4[S:4][C:5]=3[CH:6]=[N:7][CH:8]=2)=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 962WaterHCID 8028TetrahydrofuranHCID 8471TriethylamineHCID 9923070HCID 9923070, 화합물

생성물 1

HCID 70232275HCID 70232275, 화합물수율 51%

실험 절차

To a suspension of Example 131D (70 mg, 0.22 mmol) in anhydrous tetrahydrofuran (5 mL) under nitrogen atmosphere was added 1,1-carbonyldiimidazole (71 mg, 0.44 mmol) and triethylamine (60 μL, 0.44 mmol). The reaction mixture was stirred at reflux for 48 hours and then ambient temperature for an additional 24 hours. The reaction mixture was poured into a 1:1 solution of water: saturated NH4Cl and the resulting solid collected by filtration. This material was purified by flash chromatography on silica gel eluting with 20% acetone-hexane. The desired fractions were combined, evaporated and slurried in hot EtOAC to obtain title compound (39 mg) in 51% yield.

후처리

  1. temperatureat reflux for 48 hours
  2. filtrationsaturated NH4Cl and the resulting solid collected by filtration
  3. customThis material was purified by flash chromatography on silica gel eluting with 20% acetone-hexane
  4. customevaporated

출처 및 근거

ORD 기록
ord-55d7b56c8e164b2283fe89a5e22e4225
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06232320B1

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