Tetrahydrofuran → HCID 68524621, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:18]=[CH:17][CH:16]=[CH:15][C:4]=1[O:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]([OH:12])=O)=[CH:8][CH:7]=1.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>>[CH2:59]([C:52]1[CH:51]=[C:50]([CH2:49][OH:48])[S:54][C:53]=1[C:55]1[N:57]=[C:10]([C:9]2[CH:8]=[CH:7][C:6]([O:5][C:4]3[CH:15]=[CH:16][CH:17]=[CH:18][C:3]=3[O:2][CH3:1])=[CH:14][CH:13]=2)[O:12][N:56]=1)[CH3:60]Participants
Reactant 6
Product 1
Procedure
The crude product of the title compound was synthesized by conducting the reaction similar to that mentioned in Example 12 (12a) using 4-(2-methoxyphenoxy)benzoic acid (0.13 g, 0.53 mmol) that was obtained in Example 21 (21a), 1-hydroxybenzotriazole (74 mg, 0.55 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.11 g, 0.55 mmol), 5-({[t-butyl(dimethyl)silyl]oxy}methyl)-3-ethyl-N′-hydroxythiophene-2-carboximidamide (0.16 g, 0.50 mmol) that was obtained in Example 10 (10d), and 1.0 M 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 (2:5) as the eluent to afford the title compound (0.15 g) in a yield of 72% as a yellowish white crystalline solid.
Workup
- customthe reaction similar to
Sources & evidence
- ORD record
- ord-02be402d64e94d6a8cfe6a9886a0a3e2
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687491B2
Reaction notes
Loading…