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HCID 10374773、化合物 → 3-(4-(3(S)-(2(S),3-Dihydroxypropanoyl)pyrrolidin-1-yl)-3-fluorophenyl)-5(S)-(isoxazol-3-ylaminomethyl)oxazolidin-2-one

HRID 1582350
ノート
印刷プレビュー

反応式

HRID 1582350 の反応式
Cl.N[C@H:3]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][C:11]([N:14]3[CH2:18][C@H:17]([CH2:19][N:20]([C:29]4[CH:33]=[CH:32][O:31][N:30]=4)C(OCC(Cl)(Cl)Cl)=O)[O:16][C:15]3=[O:34])=[CH:10][C:9]=2[F:35])[CH2:4]1.CC1(C)[O:41][C@H:40]([C:42](Cl)=[O:43])[CH2:39][O:38]1>N1C=CC=CC=1.ClCCl.C(OCC)(=O)C.O>[OH:41][C@@H:40]([CH2:42][OH:43])[C:39]([C@H:3]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][C:11]([N:14]3[CH2:18][C@H:17]([CH2:19][NH:20][C:29]4[CH:33]=[CH:32][O:31][N:30]=4)[O:16][C:15]3=[O:34])=[CH:10][C:9]=2[F:35])[CH2:4]1)=[O:38]
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 2

HCID 10374773HCID 10374773、化合物HCID 695849253-(4(3(S) aminopyrrolidin-1-yl)-3-fluorophenyl)-5(R)-(N-(2,2,2-trichloroethyloxycarbonyl)isoxazol-3-ylaminomethyl)oxazolidin-2-one hydrochloride salt

生成物 1

HCID 537427063-(4-(3(S)-(2(S),3-Dihydroxypropanoyl)pyrrolidin-1-yl)-3-fluorophenyl)-5(S)-(isoxazol-3-ylaminomethyl)oxazolidin-2-one収率 143.5%

試薬・触媒・溶媒 4

HCID 962Water溶媒
HCID 1049
Pyridine
溶媒
HCID 6344Dichloromethane溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

3-(4-(3(S)-Aminopyrrolidin-1-yl)-3-fluorophenyl)-5(R)-(N-(2,2,2-trichloroethyloxycarbonyl)isoxazol-3-ylaminomethyl)oxazolidin-2-one hydrochloride salt (400 mg, 0.698 mM) in pyridine (5 ml) was treated dropwise with a solution of 2,2-dimethyl-1,3-dioxolan-4(S)-ylcarbonyl chloride (200 mg, 1.2 mM) in dichloromethane (2 ml), and the mixture stirred 3 hours at ambient temperature. The mixture was diluted with ethyl acetate (15 ml) and water (15 ml), the organic layer separated, washed with aqueous sodium bicarbonate (10 ml) and brine (10 ml), and evaporated, then azeotroped with toluene (20 ml). The residue was purified by chromatography on a 10 g silica Mega Bond Elut® column, eluting with a gradient increasing in polarity from 0 to 100% ethyl acetate in dichloromethane. Relevant fractions were combined and evaporated to give the desired product (435 mg ). NMR (DMSO-d6) δ: 1.30 (s, 3H); 1.37 (s, 3H); 1.89 (hextet, 1H); 2.13 (hextet, 1H); 3.20 (m, 1H); 3.24 (m overlapped by H2O, ˜1H); 3.39 (m, 1H); 3.48 (m, 1H); 3.82 (dd, 1H); 3.91 (dd, 1H); 4.12 (overlapping m, 3H); 4.33 (t overlapping m, 2H); 4.42 (dd, 2H); 4.97 (d, 1H); 5.02 (m, 1H); 5.06 (d, 1H); 6.75 (t, 1H); 6.87 (d, 1H); 7.08 (dd, 1H); 7.34 (dd, 1H); 7.94 (d, 1H); 8.89 (d, 1H). MS (ESP): 664 (MH+) for C26H29Cl3FN5O8

後処理

  1. customthe organic layer separated
  2. washwashed with aqueous sodium bicarbonate (10 ml) and brine (10 ml)
  3. customevaporated
  4. customazeotroped with toluene (20 ml)
  5. customThe residue was purified by chromatography on a 10 g silica Mega Bond Elut® column
  6. washeluting with
  7. temperaturea gradient increasing in polarity from 0 to 100% ethyl acetate in dichloromethane
  8. customevaporated

出典と根拠

ORDレコード
ord-60f8976518734c72bc0496aedeb2b5bd
出典データセット
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06734200B1

反応ノート

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