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Isoamyl Nitrite → Z-Ser-Leu-Ser-OCH3

HRID 1632419
ノート
印刷プレビュー

反応式

HRID 1632419 の反応式
[NH:1]([C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10])[C@H:2]([C:5]([NH:7]N)=[O:6])[CH2:3][OH:4].Cl.O1CCOCC1.N(OCCC(C)C)=O.[N-]=[N+]=[N-].N[C@H:38]([C:43]([NH:45][C@H:46]([C:49]([O:51][CH3:52])=[O:50])[CH2:47][OH:48])=[O:44])[CH2:39][CH:40]([CH3:42])[CH3:41].Cl>CN(C)C=O.NN.O.C(N(CC)CC)C>[NH:1]([C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10])[C@H:2]([C:5]([NH:7][C@H:38]([C:43]([NH:45][C@H:46]([C:49]([O:51][CH3:52])=[O:50])[CH2:47][OH:48])=[O:44])[CH2:39][CH:40]([CH3:42])[CH3:41])=[O:6])[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

10

反応物 5

HCID 8053Isoamyl NitriteHCID 33558AzideHCID 7016357(S)-Benzyl (1-hydrazinyl-3-hydroxy-1-oxopropan-2-yl)carbamateHCID 13875640H-Leu-Ser-OCH3.HClHCID 204431481,4-Dioxane hydrochloride

生成物 1

HCID 91978513Z-Ser-Leu-Ser-OCH3

試薬・触媒・溶媒 4

HCID 962Water溶媒
HCID 6228Dimethylformamide溶媒3 回
HCID 8471Triethylamine溶媒2 回
HCID 9321Hydrazine溶媒

反応条件

温度
-15 °C

実験手順

3.19 Grams of Z-Ser-NHNH2 was dissolved in 25 ml of dimethylformamide, and 6.30 ml of 6N-hydrochloric acid/dioxane was added to the solution, cooled to -15° C., then 1.69 ml of isoamyl nitrite was added thereto. After the reaction mixture shows a negative reaction in hydrazine-test, 1.76 ml of a cold dimethylformamide solution with 5.29 ml of triethylamine was added drop by drop in small amount to neutralize the reaction mixture. This reaction mixture containing an azide product was added to 20 ml of a cold dimethylformamide solution containing H-Leu-Ser-OCH3.HCl obtained in the above-mentioned step 14(a) and 1.60 ml of triethylamine, and the whole mixture was stirred at -10° to -15° C. for 2 hours, next at 4° C. for 18 hours. Dimethylformamide was removed by distillation under a reduced pressure, the residue obtained was solidified by adding water, reprecipitated from methanol-ethyl acetate to obtain 4.11 g of the desired product.

後処理

  1. additionwas added drop by drop in small amount
  2. customDimethylformamide was removed by distillation under a reduced pressure
  3. customthe residue obtained
  4. customreprecipitated from methanol-ethyl acetate

出典と根拠

ORDレコード
ord-a293f166da0540ffa1c432bcd83609e3
出典データセット
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04474754

反応ノート

読み込み中…

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