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Ammonium Hydroxide → Ethyl [5-(5-bromo-1,3,4-thiadiazol-2-yl)-2H-tetrazol-2-yl]acetate

HRID 390364
ノート
印刷プレビュー

反応式

HRID 390364 の反応式
[Br:1][C:2]1[S:6][C:5]([C:7]([NH2:9])=O)=[N:4][N:3]=1.BrC1S[C:14]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[N:13][N:12]=1.[NH4+:21].[OH-]>C1COCC1>[Br:1][C:2]1[S:6][C:5]([C:7]2[N:9]=[N:12][N:13]([CH2:14][C:16]([O:18][CH2:19][CH3:20])=[O:17])[N:21]=2)=[N:4][N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 14923Ammonium HydroxideHCID 52987824Ethyl5-bromo-1,3,4-thiadiazole-2-carboxylateHCID 533886795-Bromo-1,3,4-thiadiazole-2-carboxamide

生成物 1

HCID 59321687Ethyl [5-(5-bromo-1,3,4-thiadiazol-2-yl)-2H-tetrazol-2-yl]acetate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

5-Bromo-1,3,4-thiadiazole-2-carboxamide To a solution of ethyl 5-bromo-1,3,4-thiadiazole-2-carboxylate in THF (1.1 M) at room temperature was added concentrated NH4OH (2.9 equiv). The mixture was stirred at room temperature overnight and a precipitate appeared in the aqueous layer. Then the volatile solvent was removed in vacuo. The resulting mixture was diluted with water and the precipitate was collected, washed with water and dried under vacuum to give the title compound.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThen the volatile solvent was removed in vacuo
  2. additionThe resulting mixture was diluted with water
  3. customthe precipitate was collected
  4. washwashed with water
  5. customdried under vacuum

出典と根拠

ORDレコード
ord-1a60d4d36d3c46b6a0cdb654362e0959
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08383643B2

反応ノート

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