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Hydrochloric Acid → 2-((S)-2-{(R)-4-[4-((R)-2,3-dihydroxy-propoxy)-phenyl]-2,5-dioxo-imidazolidin-1-yl}-3-phenyl-propionylamino)-thiazole-4-carboxylic acid methyl ester

HRID 2222981
ノート
印刷プレビュー

反応式

HRID 2222981 の反応式
[CH3:1][O:2][C:3]([C:5]1[N:6]=[C:7]([NH:10][C:11](=[O:45])[C@@H:12]([NH:20][C:21](=[O:44])[C@H:22]([NH2:43])[C:23]2[CH:28]=[CH:27][C:26]([O:29][CH2:30][C@H:31]([O:38][Si](C)(C)C)[CH2:32][O:33][Si](C)(C)C)=[CH:25][CH:24]=2)[CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[S:8][CH:9]=1)=[O:4].C(N(C(C)C)CC)(C)C.[O:55]=[C:56](Cl)OC(Cl)(Cl)Cl.Cl.C(=O)(O)[O-].[Na+]>ClCCl.C(OCC)(=O)C.O1CCCC1>[CH3:1][O:2][C:3]([C:5]1[N:6]=[C:7]([NH:10][C:11](=[O:45])[C@@H:12]([N:20]2[C:21](=[O:44])[C@@H:22]([C:23]3[CH:28]=[CH:27][C:26]([O:29][CH2:30][C@H:31]([OH:38])[CH2:32][OH:33])=[CH:25][CH:24]=3)[NH:43][C:56]2=[O:55])[CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[S:8][CH:9]=1)=[O: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

9

反応物 5

HCID 313Hydrochloric AcidHCID 10426DiphosgeneHCID 81531DiisopropylethylamineHCID 516892Sodium BicarbonateHCID 866040572-((S)-2-{(R)-2-amino-2-[4-((S)-2,3-bis-trimethylsilanyloxy-propoxy)-phenyl]-acetylamino}-3-phenyl-propionylamino)-thiazole-4-carboxylic acid methyl ester

生成物 1

HCID 58615468
2-((S)-2-{(R)-4-[4-((R)-2,3-dihydroxy-propoxy)-phenyl]-2,5-dioxo-imidazolidin-1-yl}-3-phenyl-propionylamino)-thiazole-4-carboxylic acid methyl ester
収率 52.6%

試薬・触媒・溶媒 3

HCID 6344Dichloromethane溶媒2 回HCID 8028Tetrahydrofuran溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
0 °C

実験手順

2-((S)-2-{(R)-2-Amino-2-[4-((S)-2,3-bis-trimethylsilanyloxy-propoxy)-phenyl]-acetylamino}-3-phenyl-propionylamino)-thiazole-4-carboxylic acid methyl ester (100 mg, 0.15 mmol) and diisoproylethylamine (0.078 ml, 0.45 mmol) in dichloromethane (2 mL) were added to a solution of diphosgene (0.0143 ml, 0.12 mmol) in dichloromethane (2 mL) over 10 minute at 0° C. The mixture was stirred at 0° C. for 20 minute, diluted with ethyl acetate, washed with saturated sodium bicarbonate, brine and dried over sodium sulfate. Evaporation of solvents gave an oil which was dissolved in tetrahydrofuran (2 mL), treated with 1 N aqueous hydrochloric acid (0.45 ml, 0.45 mmol) and stirred for 3 hours. The reaction was neutralized with saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The organic extracts were washed with brine and dried over magnesium sulfate. The crude product was purified by chromatography over silica gel gradient eluted with 100% ethyl acetate up to 3% v/v methanol in ethyl acetate to give 2-((S)-2-{(R)-4-[4-((R)-2,3-dihydroxy-propoxy)-phenyl]-2,5-dioxo-imidazolidin-1-yl}-3-phenyl-propionylamino)-thiazole-4-carboxylic acid methyl ester as a solid (35 mg, 42%).

後処理

  1. washwashed with saturated sodium bicarbonate, brine
  2. dry with materialdried over sodium sulfate
  3. customEvaporation of solvents
  4. customgave an oil which
  5. stirringstirred for 3 hours
  6. extractionextracted with ethyl acetate
  7. washThe organic extracts were washed with brine
  8. dry with materialdried over magnesium sulfate
  9. customThe crude product was purified by chromatography over silica gel gradient
  10. washeluted with 100% ethyl acetate up to 3% v/v methanol in ethyl acetate

出典と根拠

ORDレコード
ord-11b9614a0a3547a79e84c1b3abebb4ee
出典データセット
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07371869B2

反応ノート

読み込み中…

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