反応式
CO[C:3](=[O:16])[C:4]1[CH:9]=[CH:8][N:7]=[C:6]([C:10]2[O:14][N:13]=[C:12]([CH3:15])[CH:11]=2)[CH:5]=1.COC(=O)C1C=CN=C(I)C=1.C[Si](C#C)(C)C.C([O-])([O-])=O.[K+].[K+].C1C(=O)N(Cl)C(=O)C1.C(=NO)C.[C:52]([O:55][C:56]([CH3:59])([CH3:58])[CH3:57])(=[O:54])[CH3:53].[Li]>CO.C(Cl)(Cl)Cl.N1C=CC=CC=1.CCN(CC)CC>[C:56]([O:55][C:52](=[O:54])[CH2:53][C:3]([C:4]1[CH:9]=[CH:8][N:7]=[C:6]([C:10]2[O:14][N:13]=[C:12]([CH3:15])[CH:11]=2)[CH:5]=1)=[O:16])([CH3:59])([CH3:58])[CH3:57]参加物
12
反応物 7
生成物 1
試薬・触媒・溶媒 4
実験手順
The title compound was prepared from 2-(3-methyl-isoxazol-5-yl)-isonicotinic acid methyl ester [prepared by i.) reaction of 2-iodo-isonicotinic acid methyl ester [CAS-No. 134579-47-8] with trimethylsilylacetylene according to general procedure H; ii.) desilylation by reaction with cat. K2CO3 in MeOH at 0° C. for 4 h; iii.) cycloadditon with a mixture of NCS, acetaldoxime, Et3N and cat. amount of pyridine in CHCl3 at 50° C. according to Tetrahedron 1984, 40, 2985-2988] by treatment with lithium tert.-butyl acetate according to general procedure K (method b). Obtained as a brown solid (5.17 g).
後処理
- customprepared by i
- custom) desilylation by reaction with cat
- customat 50° C.
出典と根拠
- ORDレコード
- ord-ecde33b9de96434a94df97d29cff0ae0
- 出典データセット
- uspto-grants-2003_04
- 特許番号
- US06544985B2
関連ノート
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