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Methanol → HCID 53327038, 화합물

HRID 2402332
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HRID 2402332 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[O:12][C:11]([C:13](Cl)=[O:14])=[CH:10][CH:9]=1.[NH2:16][C:17]1[O:18][C:19]([C:22]2[O:23][CH:24]=[CH:25][CH:26]=2)=[N:20][N:21]=1.CO>N1C=CC=CC=1>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[O:12][C:11]([C:13]([NH:16][C:17]2[O:18][C:19]([C:22]3[O:23][CH:24]=[CH:25][CH:26]=3)=[N:20][N:21]=2)=[O:14])=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 2021855-(Furan-2-yl)-1,3,4-oxadiazol-2-amineHCID 35305595-(2-fluorophenyl)furan-2-carbonyl Chloride

생성물 1

HCID 53327038HCID 53327038, 화합물수율 70%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Commercially available 5-(2-fluorophenyl)-2-furancarbonyl chloride (93 mg, 0.41 mmol) was added to a solution of commercially available 2-amino-5-(2-furyl)-1,3,4-oxadiazole (50 mg, 0.33 mmol) in pyridine (1.3 mL) under ice-cooling, followed by stirring at room temperature for 2.5 hr and then at 60° C. for 2 hr. Methanol was added to the reaction solution. The solvent was distilled off, and water was added to the residue. The precipitated crystals were collected by filtration, washed with water, methanol, and ethyl acetate sequentially, and then dried to obtain the title compound (77 mg, 0.23 mmol) (yield: 70%).

후처리

  1. temperaturecooling
  2. waitat 60° C. for 2 hr
  3. distillationThe solvent was distilled off
  4. additionwater was added to the residue
  5. filtrationThe precipitated crystals were collected by filtration
  6. washwashed with water, methanol, and ethyl acetate sequentially
  7. customdried

출처 및 근거

ORD 기록
ord-3b2278b15ce34eb88e02ac12a426827c
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08796320B2

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