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Water → HCID 54339944、化合物

HRID 745621
ノート
印刷プレビュー

反応式

HRID 745621 の反応式
CC(C)([O-])C.[K+].COP([CH2:13][C:14]([O:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:15])(OC)=O.[CH3:24][NH:25][C:26](=[O:46])[C@H:27]([CH2:37][C:38]1[CH:43]=[CH:42][C:41]([O:44][CH3:45])=[CH:40][CH:39]=1)[NH:28][C:29](=[O:36])[C:30](=O)[CH2:31][CH:32]([CH3:34])[CH3:33].O>CN(C)C=O>[CH3:24][NH:25][C:26](=[O:46])[C@H:27]([CH2:37][C:38]1[CH:39]=[CH:40][C:41]([O:44][CH3:45])=[CH:42][CH:43]=1)[NH:28][C:29](=[O:36])[C:30]([CH2:31][CH:32]([CH3:33])[CH3:34])=[CH:13][C:14]([O:16][CH2:17][C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)=[O:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 2773759Benzyl DimethylphosphonoacetateHCID 14303083N-(4-Methyl-2-oxopentanoyl)-O-methyl-L-tyrosine N-MethylamideHCID 23665647Potassium tert-butoxide

生成物 1

HCID 54339944HCID 54339944、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

Potassium tertiary butoxide (2.1 g., 0.0188 mol.) was suspended in dry dimethylformamide (50 mls.). To the suspension was added benzyl dimethylphosphonoethanoate (4.6 g., 0.0187 mol.) at room temperature. The reaction mixture was stirred at room temperature for 0.5 hours. N-(4-Methyl-2-oxopentanoyl)-O-methyl-L-tyrosine N-Methylamide (3.0 g., 0.00913 mol) was added portionwise to the reaction mixture over a period of 10 minutes to yield a red solution. The red solution was stirred at room temperature for 4 hours, and then poured into water (500 mls.). The resulting mixture obtained was extracted with ethyl acetate (2×100 mls.) and the ethyl acetate extract was washed with water (2×25 mls.), brine (25 mls.) and dried over anhydrous magnesium sulfate. The ethyl acetate was removed by evaporation in vacuo to yield a crude solid product (4.2 g.). The crude product was purified by recrystallization from a mixture of ethyl acetate and hexane to yield E and Z N-[3-(benzyloxycarbonyl)-2-(2-methylpropyl)propenoyl]-O-methyl-L-tyrosine N-methylamide as a light brown crystalline solid. (m.p. 167°-9° C. Found: C, 68.3; H, 7.1; N, 6.3 %. C25H30N2O5 requires C, 68.5; H, 6.9; N, 6.4%).

後処理

  1. customto yield a red solution
  2. stirringThe red solution was stirred at room temperature for 4 hours
  3. customThe resulting mixture obtained
  4. extractionwas extracted with ethyl acetate (2×100 mls.)
  5. extractionthe ethyl acetate extract
  6. washwas washed with water (2×25 mls.), brine (25 mls.)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customThe ethyl acetate was removed by evaporation in vacuo
  9. customto yield a crude solid product (4.2 g.)
  10. customThe crude product was purified by recrystallization from a mixture of ethyl acetate and hexane

出典と根拠

ORDレコード
ord-b505a2b4fed242cda9e58937f8bf82ca
出典データセット
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04599361

反応ノート

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