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4-Methylmorpholine → BOC-MePhe-NHCH2CH2CH2NMe2

HRID 1447804
ノート
印刷プレビュー

反応式

HRID 1447804 の反応式
[C:1]([O:5][C:6]([N:8]([CH3:20])[C@H:9]([C:17]([OH:19])=O)[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CN1CCOCC1.[NH2:28][CH2:29][CH2:30][CH2:31][N:32]([CH3:34])[CH3:33]>ClCCl>[C:6]([N:8]([CH3:20])[C@H:9]([C:17]([NH:28][CH2:29][CH2:30][CH2:31][N:32]([CH3:34])[CH3:33])=[O:19])[CH2:10][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7]
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 79724-MethylmorpholineHCID 7993N,N-Dimethyl-1,3-propanediamineHCID 7010602Boc-N-Me-Phe-OH

生成物 1

HCID 131711662BOC-MePhe-NHCH2CH2CH2NMe2

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

N-t-Butyloxycarbonyl-N-methylphenylalanine (2.79 g) and NMM (1.01 g) were dissolved in dichloromethane (20 ml) and the stirred solution cooled to -20° IBCF (1.37 g) was then added and the mixture stirred for 5 minutes before the addition of NH2CH2CH2CH2NMe2 (1.02 g). The solution was stirred for 1 hour at -20° and then at room temperature for 12 hours. The mixture was evaporated, and the residue dissolved in ethyl acetate (50 ml) and an aqueous solution of sodium bicarbonate (saturated, 50 ml). The ethyl acetate layer was washed with aqueous sodium bicarbonate (saturated, 50 ml), water (2×50 ml) and 10% aqueous citric acid (2×50 ml). The citric acid extracts were combined, made basic with saturated sodium bicarbonate solution, and extracted with ethyl acetate (3×50 ml). The ethyl acetate extracts were combined, dried (Na2SO4) and evaporated to yield the title compound as an oil Rf1E 0.24, Rf3A 0.37.

後処理

  1. temperaturethe stirred solution cooled to -20° IBCF (1.37 g)
  2. additionwas then added
  3. waitat room temperature for 12 hours
  4. customThe mixture was evaporated
  5. dissolutionthe residue dissolved in ethyl acetate (50 ml)
  6. washThe ethyl acetate layer was washed with aqueous sodium bicarbonate (saturated, 50 ml), water (2×50 ml) and 10% aqueous citric acid (2×50 ml)
  7. extractionextracted with ethyl acetate (3×50 ml)
  8. dry with materialdried (Na2SO4)
  9. customevaporated

出典と根拠

ORDレコード
ord-f00e84a52ab6457ab47b7b92b699c88c
出典データセット
uspto-grants-1979_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04178371

反応ノート

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