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Triethylamine → HCID 13945819、化合物

HRID 1252838
ノート
印刷プレビュー

反応式

HRID 1252838 の反応式
[C:1]1([CH2:7][CH2:8][P:9](=O)([O:18]CC2C=CC=CC=2)[O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Cl)(Cl)(Cl)(Cl)Cl.[C:33]1([CH2:39][O:40][C:41]([NH:43][CH2:44][CH2:45][CH2:46][CH2:47][C@H:48]([OH:66])[C:49]([N:51]2[CH2:65][CH2:64][CH2:63][C@H:52]2[C:53]([O:55][CH2:56][C:57]2[CH:62]=[CH:61][CH:60]=[CH:59][CH:58]=2)=[O:54])=[O:50])=[O:42])[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1.C(N(CC)CC)C.CN(C1C=CC=CN=1)C>C1C=CC=CC=1>[C:1]1([CH2:7][CH2:8][P:9]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)([O:66][C@@H:48]([CH2:47][CH2:46][CH2:45][CH2:44][NH:43][C:41]([O:40][CH2:39][C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)=[O:42])[C:49]([N:51]2[CH2:65][CH2:64][CH2:63][C@H:52]2[C:53]([O:55][CH2:56][C:57]2[CH:62]=[CH:61][CH:60]=[CH:59][CH:58]=2)=[O:54])=[O:50])=[O:18])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 8471TriethylamineHCID 218852-DimethylaminopyridineHCID 24819Phosphorus pentachlorideHCID 13630870Dibenzyl (2-phenylethyl)phosphonateHCID 13934652HCID 13934652、化合物

生成物 1

HCID 13945819HCID 13945819、化合物

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

A mixture of (2-phenylethyl)phosphonic acid, dibenzyl ester (1.48 g., 4.04 mmole, 1.5 eq.) in dry benzene (15 ml.) is treated with phosphorus pentachloride (952 mg., 4.57 mmole, 1.7 eq.) and the solution is heated at 75° (oil bath) for 2.5 hours under argon. The mixture is evaporated to dryness (0.5 mm of Hg.), taken up in benzene (10 ml.), and evaporated. This procedure is repeated twice. The clear residue is taken up in dry methylene chloride (15 ml.), 1-[(S)-6-[[(phenylmethoxy)carbonyl]amino]-2-hydroxy-1-oxohexyl]-L-proline, phenylmethyl ester (1.26 g., 2.69 mmole, 1.0 eq.) is added, the mixture is cooled to 0° (ice-bath), then treated with triethylamine (0.56 ml., 4.04 mmole, 1.5 eq.) and dimethylaminopyridine (49 mg., 0.40 mmole, 0.15 eq.), stirred at 0° for 15 minutes, and then at room temperature for one hour. The mixture is partitioned between 5% potassium bisulfate and methylene chloride. The organic layer is washed with brine, dried over anhydrous sodium sulfate, and evaporated to a yellow oil. The crude oil is purified by flash chromatography (LPS-1 silica gel) eluting with hexane:acetone (7:3). Product containing fractions are pooled and evaporated to give 916 mg. of 1-[(S)-2-[[(2-phenylethyl)(phenylmethoxy)phosphinyl]oxy]-6-[[((phenylmethoxy)carbonyl]amino]-1-oxohexyl]-L-proline, phenylmethyl ester as a clear, colorless oil.

後処理

  1. temperaturethe solution is heated at 75° (oil bath) for 2.5 hours under argon
  2. customThe mixture is evaporated to dryness (0.5 mm of Hg.)
  3. customevaporated
  4. temperaturethe mixture is cooled to 0° (ice-bath)
  5. waitat room temperature for one hour
  6. customThe mixture is partitioned between 5% potassium bisulfate and methylene chloride
  7. washThe organic layer is washed with brine
  8. dry with materialdried over anhydrous sodium sulfate
  9. customevaporated to a yellow oil
  10. customThe crude oil is purified by flash chromatography (LPS-1 silica gel)
  11. washeluting with hexane:acetone (7:3)
  12. additionProduct containing fractions
  13. customevaporated
  14. customto give 916 mg

出典と根拠

ORDレコード
ord-fc2f70e249154c2a880cf51beb78135d
出典データセット
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04745196

反応ノート

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