N,N-Dimethylbenzamide → 4-Thiazolecarboxylic acid

HRID 1181174

反応式

HRID 1181174 の反応式
P([O-])([O-])([O-])=O.[K+].[K+].[K+].[S:9]1[CH:13]=[C:12]([C:14]#[N:15])[N:11]=[CH:10]1.C(#N)C.[OH2:19].CN(C)[C:22](=[O:29])[C:23]1[CH:28]=CC=CC=1>C(#N)C>[S:9]1[CH:13]=[C:12]([C:14]([NH2:15])=[O:29])[N:11]=[CH:10]1.[S:9]1[CH:28]=[C:23]([C:22]([OH:29])=[O:19])[N:11]=[CH:10]1

参加物

7

反応物 4

HCID 11916N,N-DimethylbenzamideHCID 150694-Cyanothiazole3 回HCID 62657Potassium Phosphate, TribasicHCID 18373917Acetonitrile--water (1/1)

生成物 2

HCID 3042714-Thiazolecarboxylic acidHCID 4452761,3-Thiazole-4-carboxamide

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a 15-mL polypropylene centrifuge tube is added 3.70 mL of 50 mM potassium phosphate buffer (pH 7.0), 1.0 mL of a suspension of 22.1 mg dry cell weight E. coli SW132 wet cells (prepared as described in Example 10) in 50 mM potassium phosphate buffer (pH 7.0), and 0.2754 g of 4-thiazolecarbonitrile. The final concentration of 4-thiazolecarbonitrile is 0.500 M. The reaction mixture is mixed on a rotating platform at 25° C. After 30 min, 7.50 mL of 95:5 acetonitrile/water containing 0.30 M N,N-dimethylbenzamide (HPLC external standard) is added to the reaction, the resulting mixture centrifuged, and a 0.100 mL of the supernatant mixed with 0.900 mL of acetonitrile and analyzed by HPLC. The conversion of 4-thiazolecarbonitrile is 100%, and the yields of 4-thiazolecarboxamide and 4-thiazolecarboxylic acid are 100% and 0%, respectively.

後処理

  1. customdry cell weight E
  2. customwet cells (prepared as described in Example 10) in 50 mM potassium phosphate buffer (pH 7.0)
  3. additionThe reaction mixture is mixed on a rotating platform at 25° C

出典と根拠

ORDレコード
ord-a354450271cc45119fcd655a8a0867cd
出典データセット
uspto-grants-2007_10
特許番号
US07285406B2

関連ノート

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