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Citric Acid → N-[4-[4-(2,4-diamino-6-methyl-5-pyrimidinyl)-1-piperazinyl]benzoyl]-L-glutamic acid

HRID 371457
ノート
印刷プレビュー

反応式

HRID 371457 の反応式
C([O:3][C:4](=[O:37])[C@H:5]([CH2:30][CH2:31][C:32]([O:34]CC)=[O:33])[NH:6][C:7](=[O:29])[C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH2:19][CH2:18][N:17]([C:20]3[C:21]([NH2:28])=[N:22][C:23]([NH2:27])=[N:24][C:25]=3[CH3:26])[CH2:16][CH2:15]2)=[CH:10][CH:9]=1)C.[OH-].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CO>[NH2:27][C:23]1[N:22]=[C:21]([NH2:28])[C:20]([N:17]2[CH2:16][CH2:15][N:14]([C:11]3[CH:10]=[CH:9][C:8]([C:7]([NH:6][C@H:5]([C:4]([OH:37])=[O:3])[CH2:30][CH2:31][C:32]([OH:34])=[O:33])=[O:29])=[CH:13][CH:12]=3)[CH2:19][CH2:18]2)=[C:25]([CH3:26])[N:24]=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 311Citric AcidHCID 14798Sodium HydroxideHCID 13478337N-[4-[4-(2,4-Diamino-6-methyl-5-pyrimidinyl)-1-piperazinyl]benzoyl]-L-glutamic acid diethyl ester

生成物 1

HCID 13478336N-[4-[4-(2,4-diamino-6-methyl-5-pyrimidinyl)-1-piperazinyl]benzoyl]-L-glutamic acid収率 28.3%

試薬・触媒・溶媒 1

HCID 887Methanol
溶媒

実験手順

A mixture of 3.00 g (0.0058 mole) of N-[4-[4-(2,4-diamino-6-methyl-5-pyrimidinyl)-1-piperazinyl]-benzoyl]-L-glutamic acid diethyl ester and 12.5 ml of 1N aqueous sodium hydroxide solution in 150 ml of methanol was stirred at room temperature for four hours. The methanol was removed under vacuum at 23° C. and the residue was dissolved in 100 ml of ice water and then neutralized by the addition of 2.5 g (0.0129 moles) of citric acid. The solid precipitate was collected, washed with water, and then triturated several times with ethanol. The remaining solid was dried overnight in vacuo at 67° C. to give 0.75 g of the product as a white powder, mp 270° C. (dec.).

後処理

  1. customThe methanol was removed under vacuum at 23° C.
  2. dissolutionthe residue was dissolved in 100 ml of ice water
  3. customThe solid precipitate was collected
  4. washwashed with water
  5. customtriturated several times with ethanol
  6. customThe remaining solid was dried overnight in vacuo at 67° C.

出典と根拠

ORDレコード
ord-b329b7b11ee34d3c9679794b347d968c
出典データセット
uspto-grants-1985_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04532240

反応ノート

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