Ethylmorpholine → HCID 53667817、化合物

HRID 1448742ノート

反応式

HRID 1448742 の反応式
[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:14]([N:16]1[CH2:23][CH2:22][CH2:21][C@H:17]1[C:18]([OH:20])=O)=[O:15])[CH3:13])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N1CCOCC1)C.ClC(OCC(C)C)=O.[CH2:40]([NH2:45])[CH2:41][CH2:42][CH2:43][CH3:44]>O1CCCC1>[CH2:40]([NH:45][C:18](=[O:20])[C@@H:17]1[CH2:21][CH2:22][CH2:23][N:16]1[C:14](=[O:15])[C@H:12]([CH3:13])[NH:11][C:9]([O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[O:10])[CH2:41][CH2:42][CH2:43][CH3:44]

参加物

6

反応物 4

HCID 7525EthylmorpholineHCID 8060PentylamineHCID 62365Isobutyl chloroformateHCID 5388928Z-Ala Prolinal

生成物 1

HCID 53667817HCID 53667817、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-10 °C

実験手順

2 g (0.06 mol) of N-benzyloxycarbonyl-L-alanyl-L-proline were dissolved in 20 ml of dry tetrahydrofuran and the solution was cooled to -10° C. 0.76 ml (0.06 mol) of N-ethylmorpholine and 0.79 ml (0.006 mol) of isobutyl chloroformate were added and the resulting mixture was stirred at -10° C. for 20 minutes. 0.69 ml (0.006 mol) of n-pentylamine was then added and the resulting solution was stirred at -20° C. for 1 hour and then left to stand at room temperature overnight. The solution was then evaporated to an oil which was dissolved in ethyl acetate. The ethyl acetate solution was washed twice with water, twice with 5% citric acid solution, once with water, twice with 5% sodium bicarbonate solution and twice with water, dried and evaporated to an oil. The desired N-benzyloxycarbonyl-L-alanyl-L-proline n-pentylamide was crystallised from ethyl acetate/petroleum ether in a yield of 1 g (42.8%) and with a melting point of 102°-104° C.

後処理

  1. stirringthe resulting solution was stirred at -20° C. for 1 hour
  2. waitleft
  3. waitto stand at room temperature overnight
  4. customThe solution was then evaporated to an oil which
  5. dissolutionwas dissolved in ethyl acetate
  6. washThe ethyl acetate solution was washed twice with water, twice with 5% citric acid solution, once with water, twice with 5% sodium bicarbonate solution and twice with water
  7. customdried
  8. customevaporated to an oil
  9. customThe desired N-benzyloxycarbonyl-L-alanyl-L-proline n-pentylamide was crystallised from ethyl acetate/petroleum ether in a yield of 1 g (42.8%) and with a melting point of 102°-104° C.

出典と根拠

ORDレコード
ord-38d44c2166d345b7b08f7956245d1798
出典データセット
uspto-grants-1980_02
特許番号
US04187216

反応ノート

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