Tetrahydrofuran → (5-{5-[3-Chloro-4-(3-fluorophenoxy)phenyl]-1,2,4-oxadiazol-3-yl}-4-ethyl-2-thienyl)methanol

HRID 2247712노트

반응식

HRID 2247712 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=1)[C:5]([OH:7])=O.ON1C2C=CC=CC=2N=N1.Cl.C(N=C=NCCCN(C)C)C.[Si]([O:48][CH2:49][C:50]1[S:54][C:53]([C:55](=[N:57]O)[NH2:56])=[C:52]([CH2:59][CH3:60])[CH:51]=1)(C(C)(C)C)(C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC.O1CCCC1>>[Cl:1][C:2]1[CH:3]=[C:4]([C:5]2[O:7][N:57]=[C:55]([C:53]3[S:54][C:50]([CH2:49][OH:48])=[CH:51][C:52]=3[CH2:59][CH3:60])[N:56]=2)[CH:8]=[CH:9][C:10]=1[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=1

참가 물질

7

실험 절차

The crude product of the title compound was synthesized by conducting the reaction similar to that mentioned in Example 5 (5a) using 3-chloro-4-(3-fluorophenoxy)benzoic acid (0.14 g, 0.53 mmol) that was obtained in Example 16 (16a), 1-hydroxybenzotriazole (0.086 g, 0.56 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.11 g, 0.56 mmol), 5-({[t-butyl(dimethyl)silyl]oxy}methyl)-3-ethyl-N′-hydroxythiophene-2-carboximidamide (0.16 g, 0.51 mmol) that was obtained in Example 10 (10d), and 1.0M solution of tetrabutylammoniumfluoride in tetrahydrofuran (1.0 mL, 1.0 mmol). Subsequently, the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (2:8 to 5:5) as the eluent to afford the title compound (0.17 g) in a yield of 89% as a pale yellowish crystalline solid.

후처리

  1. customthe reaction similar to

출처 및 근거

ORD 기록
ord-fff068e8a2244f0b9e0fb9b52d8ee061
출처 데이터셋
uspto-grants-2010_03
특허 번호
US07687491B2

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