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Methyl tyrosinate hydrochloride → Folic acid tyrosine methyl ester

HRID 1156490
ノート
印刷プレビュー

反応式

HRID 1156490 の反応式
[C:1]([O-:32])(=[O:31])[CH2:2][CH2:3][C@H:4]([NH:8][C:9]([C:11]1[CH:30]=[CH:29][C:14]([NH:15][CH2:16][C:17]2[N:28]=[C:27]3[C:20]([N:21]=[C:22]([NH:24][C:25]3=[O:26])[NH2:23])=[N:19][CH:18]=2)=[CH:13][CH:12]=1)=[O:10])[C:5]([OH:7])=[O:6].[Na+].Cl.C(N=C=NCCCN(C)C)C.Cl.[CH3:47][O:48][C:49](=[O:60])[C@H:50]([CH2:52][C:53]1[CH:58]=[CH:57][C:56]([OH:59])=[CH:55][CH:54]=1)[NH2:51]>O>[CH3:47][O:48][C:49](=[O:60])[C@H:50]([CH2:52][C:53]1[CH:54]=[CH:55][C:56]([OH:59])=[CH:57][CH:58]=1)[NH2:51].[C:1]([OH:32])(=[O:31])[CH2:2][CH2:3][C@H:4]([NH:8][C:9]([C:11]1[CH:12]=[CH:13][C:14]([NH:15][CH2:16][C:17]2[N:28]=[C:27]3[C:20]([N:21]=[C:22]([NH:24][C:25]3=[O:26])[NH2:23])=[N:19][CH:18]=2)=[CH:29][CH:30]=1)=[O:10])[C:5]([OH:7])=[O:6]
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 76956Methyl tyrosinate hydrochlorideHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 136359212Sodium folate

生成物 1

HCID 136359211Folic acid tyrosine methyl ester

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

Sodium folate (100 mg.) is dissolved in water (10 ml.). To this is added 1-ethyl-3-(3 dimethylaminopropyl)carbodiimide hydrochloride (100 mg.), followed by the addition of tyrosine methyl ester hydrochloride (32 mg.) dissolved in water (2 ml.). A yellow gelatinous precipitate forms. The mixture is stirred for four hours at room temperature. The precipitated material is extracted into ethyl acetate and washed successively with 1 N sodium bicarbonate (3×10 ml.) 1 N hydrochloric acid (3×10 ml.) and water (2×10 ml.). The solution is dried over anhydrous magnesium sulfate and the ethyl acetate removed on a rotary evaporator. Trituration of the remaining residues with hexane yields yellow crystalline folic acid tyrosine methyl ester conjugate weighing 56 mg.

後処理

  1. extractionThe precipitated material is extracted into ethyl acetate
  2. washwashed successively with 1 N sodium bicarbonate (3×10 ml.) 1 N hydrochloric acid (3×10 ml.) and water (2×10 ml.)
  3. dry with materialThe solution is dried over anhydrous magnesium sulfate
  4. customthe ethyl acetate removed on a rotary evaporator

出典と根拠

ORDレコード
ord-6df24563178a4476a4b6787d8b578541
出典データセット
uspto-grants-1982_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04336185

反応ノート

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