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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Z-Ser-Tyr-OMe

HRID 1279182
ノート
印刷プレビュー

反応式

HRID 1279182 の反応式
[NH:1]([C:8]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:9])[C@H:2]([C:5]([OH:7])=O)[CH2:3][OH:4].[NH2:18][C@H:19]([C:28]([O:30][CH3:31])=[O:29])[CH2:20][C:21]1[CH:26]=[CH:25][C:24]([OH:27])=[CH:23][CH:22]=1.ON1C(=O)CCC1=O.CCN=C=NCCCN(C)C>CN(C=O)C>[NH:1]([C:8]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:9])[C@H:2]([C:5]([NH:18][C@H:19]([C:28]([O:30][CH3:31])=[O:29])[CH2:20][C:21]1[CH:22]=[CH:23][C:24]([OH:27])=[CH:25][CH:26]=1)=[O:7])[CH2:3][OH:4]
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 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 70652Tyrosine Methyl EsterHCID 80170N-HydroxysuccinimideHCID 100310N-(Benzyloxycarbonyl)-L-serine

生成物 1

HCID 13190522Z-Ser-Tyr-OMe収率 92.4%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

反応条件

温度
0 °C

実験手順

Z-Ser-OH 23.9 g and 23.2 g of H-Tyr-OMe were dissolved in 50 mL of DMF, 12.7 g of HOSu and 20 mL of WSC were added to the solution, then the mixture was stirred at 0° C. for 5 minutes then at room temperature overnight. After confirmation with ninhydrin, the reaction mixture was concentrated under reduced pressure. Ethyl acetate 500 mL was added to the residue, and the mixture was washed twice with 200 mL of 1N hydrochloric acid, twice with 200 mL of saturated aqueous sodium bicarbonate, twice with saturated saline, in this order. The ethyl acetate layer was concentrated under reduced pressure. The residue was solidified by treatment with hexane. Thus 38.44 g of Z-Ser-Tyr-OMe (92.3% yield) was obtained.

後処理

  1. customat room temperature
  2. customovernight
  3. concentrationAfter confirmation with ninhydrin, the reaction mixture was concentrated under reduced pressure
  4. additionEthyl acetate 500 mL was added to the residue
  5. washthe mixture was washed twice with 200 mL of 1N hydrochloric acid, twice with 200 mL of saturated aqueous sodium bicarbonate, twice with saturated saline, in this order
  6. concentrationThe ethyl acetate layer was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-4dc8528b1e4d48c89102bfc4c191e200
出典データセット
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06448031B1

反応ノート

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