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4-Methylmorpholine → t-Butoxycarbonylvalyltyrosine methyl ester

HRID 1395809
ノート
印刷プレビュー

反応式

HRID 1395809 の反応式
[C:1]([O:5][C:6]([NH:8][C@H:9]([C:13]([OH:15])=O)[CH:10]([CH3:12])[CH3:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].CN1CCOCC1.C(OC(Cl)=O)C(C)C.Cl.[CH3:32][O:33][C:34](=[O:45])[C@H:35]([CH2:37][C:38]1[CH:43]=[CH:42][C:41]([OH:44])=[CH:40][CH:39]=1)[NH2:36]>C(Cl)Cl>[CH3:32][O:33][C:34](=[O:45])[C@H:35]([CH2:37][C:38]1[CH:39]=[CH:40][C:41]([OH:44])=[CH:42][CH:43]=1)[NH:36][C:13](=[O:15])[C@H:9]([CH:10]([CH3:11])[CH3:12])[NH:8][C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7]
参加物反応条件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 79724-MethylmorpholineHCID 62365Isobutyl chloroformateHCID 76956Methyl tyrosinate hydrochlorideHCID 83693Boc-L-Valine

生成物 1

HCID 14752398t-Butoxycarbonylvalyltyrosine methyl ester

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-70 °C

実験手順

21.7 g of t-butoxycarbonylvaline is dissolved in 200 ml of methylene chloride. 22.2 ml of N-methylmorpholine is added to the solution. The solution is cooled to -70° C. 13.1 ml of isobutylchloroformate is then added. The reaction mixture is again cooled to -70° C. 23.2 g of tyrosine methyl ester hydrochloride is added to the reaction mixture. The reaction mixture is allowed to warm to room temperature, and then is stirred for 16 hours. The reaction mixture is extracted three times with 0.5 M potassium bisulfate and once with brine. The methylene chloride solution is dried over anhydrous sodium sulfate, filtered and stripped of solvent. The residue is dissolved in 200 ml of ethyl ether. The ether solution is added to cold rapidly stirring Skellysolve B. The white precipitate is filtered and dried to afford the product t-butoxycarbonylvalyltyrosine methyl ester.

後処理

  1. temperatureThe reaction mixture is again cooled to -70° C
  2. temperatureto warm to room temperature
  3. extractionThe reaction mixture is extracted three times with 0.5 M potassium bisulfate
  4. dry with materialThe methylene chloride solution is dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. dissolutionThe residue is dissolved in 200 ml of ethyl ether
  7. additionThe ether solution is added to cold rapidly stirring Skellysolve B
  8. filtrationThe white precipitate is filtered
  9. customdried

出典と根拠

ORDレコード
ord-2273e8eb9ebd41a58e68eaeaf23ea4ac
出典データセット
uspto-grants-1980_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04204991

反応ノート

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