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Triethylamine → 1-adamantylcarbonyl-L-alanyl-L-proline anilide

HRID 1448733
ノート
印刷プレビュー

反応式

HRID 1448733 の反応式
Br.[NH2:2][C@H:3]([C:5]([N:7]1[CH2:20][CH2:19][CH2:18][C@H:8]1[C:9]([NH:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:10])=[O:6])[CH3:4].C(N(CC)CC)C.[C:28]12([C:38](Cl)=[O:39])[CH2:37][CH:32]3[CH2:33][CH:34]([CH2:36][CH:30]([CH2:31]3)[CH2:29]1)[CH2:35]2>O1CCCC1>[C:28]12([C:38]([NH:2][C@H:3]([C:5]([N:7]3[CH2:20][CH2:19][CH2:18][C@H:8]3[C:9]([NH:11][C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)=[O:10])=[O:6])[CH3:4])=[O:39])[CH2:35][CH:34]3[CH2:33][CH:32]([CH2:31][CH:30]([CH2:36]3)[CH2:29]1)[CH2:37]2
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

5

反応物 3

HCID 8471TriethylamineHCID 989151-Adamantanecarbonyl chlorideHCID 22809936L-alanyl-L-proline anilide hydrobromide

生成物 1

HCID 322978541-adamantylcarbonyl-L-alanyl-L-proline anilide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

3.42 g (0.01 mol) of L-alanyl-L-proline anilide hydrobromide were suspended in 100 ml of dry tetrahydrofuran and the suspension was cooled to 0° C. There were then added 2.8 ml (0.02 mol) of triethylamine followed by 1.72 g (0.001 mol) of 1-adamantoyl chloride. The mixture was stirred at 0° C. for 0.5 hour and at room temperature for 2 hours and then evaporated. The residue was extracted twice with 40 ml of ethyl acetate each time. The combined ethyl acetate extracts were washed successively with two 20 ml portions of 1-N hydrochloric acid, 20 ml of water, two 20 ml portions of 5% sodium bicarbonate solution and two 20 ml portions of water, dried over magnesium sulphate and evaporated. The residue was crystallised from ether/petroleum ether and further purified by chromatography on 100 g of silica gel using chloroform for the elution. Evaporation of the chloroform eluate and crystallisation of the residue from ether/petroleum ether yielded 1.09 g (24%) of pure N-(1-adamantylcarbonyl-L-alanyl-L-proline anilide of melting point 119°-121° C.; [α]D20 =-142.9° (c=1% in methanol).

後処理

  1. customevaporated
  2. extractionThe residue was extracted twice with 40 ml of ethyl acetate each time
  3. washThe combined ethyl acetate extracts were washed successively with two 20 ml portions of 1-N hydrochloric acid, 20 ml of water, two 20 ml portions of 5% sodium bicarbonate solution and two 20 ml portions of water
  4. dry with materialdried over magnesium sulphate
  5. customevaporated
  6. customThe residue was crystallised from ether/petroleum ether
  7. customfurther purified by chromatography on 100 g of silica gel
  8. washfor the elution
  9. customEvaporation of the chloroform eluate and crystallisation of the residue from ether/petroleum ether

出典と根拠

ORDレコード
ord-d2b31c78dd014162af2c59c1170709a5
出典データセット
uspto-grants-1980_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04187216

反応ノート

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