Water → HCID 13127783、化合物

HRID 2292389ノート

反応式

HRID 2292389 の反応式
C(N(CCCC)CCCC)CCC.[S:14]1[CH:18]=[CH:17][CH:16]=[C:15]1[CH2:19][C:20]([NH:22][C@@H:23]1[C:35](=[O:36])[N:25]2[C:26]([C:32]([OH:34])=[O:33])=[C:27]([CH2:30]O)[CH2:28][S:29][C@H:24]12)=[O:21].[SH:37][C:38]1[N:42]([CH3:43])[N:41]=[N:40][N:39]=1.O>C(OCC)(=O)C>[S:14]1[CH:18]=[CH:17][CH:16]=[C:15]1[CH2:19][C:20]([NH:22][C@@H:23]1[C:35](=[O:36])[N:25]2[C:26]([C:32]([OH:34])=[O:33])=[C:27]([CH2:30][S:37][C:38]3[N:42]([CH3:43])[N:41]=[N:40][N:39]=3)[CH2:28][S:29][C@H:24]12)=[O:21]

参加物

5

反応物 3

HCID 962WaterHCID 70378458HCID 70378458、化合物HCID 178482017HCID 178482017、化合物

生成物 1

HCID 13127783HCID 13127783、化合物収率 84.1%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒2 回

反応条件

温度
-20 °C

実験手順

To 10 ml of ethyl acetate were added 0.540 g of 7β-(2-thienylacetamido)-3-hydroxymethyl-3-cephem-4-carboxylic acid tri-n-butylamine salt and 0.175 g of 5-mercapto-1-methyl-1H tetrazole and, under cooling at -20° C. and stirring, a solution of 0.370 g of methyl o-phenylene phosphorochloridate in 5 ml of ethyl acetate was added. The mixture was stirred under ice-cooling for 1.5 hours and 10 ml of water was added. After phase separation, 20 ml of water was added to the organic layer and mixture was adjusted to pH 9.0. The aqueous layer was taken and washed with 5 ml of ethyl acetate. To the aqueous layer was added 20 ml of ethyl acetate and the mixture was adjusted to pH 2.0. After phase separation, the organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. The ethyl acetate was distilled off under reduced pressure and ether was added. The powdery precipitate was collected by filtration to give 0.380 g (yield 84.1%) of 7β-(2-thienylacetamido)-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid. The IR and NMR spectra of this product were identical with those of the authentic sample.

後処理

  1. stirringThe mixture was stirred under ice-
  2. temperaturecooling for 1.5 hours
  3. customAfter phase separation, 20 ml of water
  4. additionwas added to the organic layer and mixture
  5. washwashed with 5 ml of ethyl acetate
  6. additionTo the aqueous layer was added 20 ml of ethyl acetate
  7. customAfter phase separation
  8. washthe organic layer was washed with saturated aqueous sodium chloride
  9. dry with materialdried over anhydrous sodium sulfate
  10. distillationThe ethyl acetate was distilled off under reduced pressure and ether
  11. additionwas added
  12. filtrationThe powdery precipitate was collected by filtration

出典と根拠

ORDレコード
ord-5c27c5d31cf545889d95f04f7e36d4e7
出典データセット
uspto-grants-1989_01
特許番号
US04801703

反応ノート

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