Oxygen → (2R,4R)-5-(3'-Chlorobiphenyl-4-yl)-2-hydroxy-4-[(1-hydroxy-1H-[1,2,3]triazole-4-carbonyl)-amino]pentanoic Acid

HRID 2273483ノート

反応式

HRID 2273483 の反応式
[OH:1][N:2]1[CH:6]=[C:5]([C:7]([OH:9])=O)[N:4]=[N:3]1.CN(C(ON1N=N[C:20]2[CH:21]=[CH:22][C:23](=[CH:25][C:19]1=2)[Cl:24])=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.C([O:46][C:47](=[O:61])[C@H:48]([OH:60])[CH2:49][C@H:50]([NH2:59])[CH2:51][C:52]1[CH:57]=[CH:56][C:55](Br)=[CH:54][CH:53]=1)C.ClC1C=C(B(O)O)C=CC=1.C([O-])([O-])=O.[K+].[K+].O=O>CN(C=O)C.O.CCO>[Cl:24][C:23]1[CH:25]=[C:19]([C:55]2[CH:54]=[CH:53][C:52]([CH2:51][C@@H:50]([NH:59][C:7]([C:5]3[N:4]=[N:3][N:2]([OH:1])[CH:6]=3)=[O:9])[CH2:49][C@@H:48]([OH:60])[C:47]([OH:61])=[O:46])=[CH:57][CH:56]=2)[CH:20]=[CH:21][CH:22]=1

参加物

11

反応物 7

HCID 977OxygenHCID 11430Potassium CarbonateHCID 81531DiisopropylethylamineHCID 2734323(3-Chlorophenyl)boronic acidHCID 42624899O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphateHCID 534331041-Hydroxy-1H-1,2,3-triazole-4-carboxylic AcidHCID 67969401(2R,4R)-4-amino-5-(4-bromophenyl)-2-hydroxypentanoic acid ethyl ester

生成物 1

HCID 57377989(2R,4R)-5-(3'-Chlorobiphenyl-4-yl)-2-hydroxy-4-[(1-hydroxy-1H-[1,2,3]triazole-4-carbonyl)-amino]pentanoic Acid収率 20.5%

試薬・触媒・溶媒 3

HCID 702Ethanol溶媒HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

1-Hydroxy-1H-1,2,3-triazole-4-carboxylic acid (17.6 mg, 136 μmol) and HCTU (56.4 mg, 136 μmol) were combined in DMF and stirred for 5 minutes at room temperature. DIPEA (71.2 μl, 409 μmol) and (2R,4R)-4-amino-5-(4-bromophenyl)-2-hydroxypentanoic acid ethyl ester (43 mg, 140 μmol) were added and the resulting mixture was stirred for 10 minutes. The reaction mixture was evaporated under reduced pressure and purified (C18 reverse phase column). The purified material was combined with 3-chlorophenylboronic acid, pinacol ester (48.1 mg, 202 μmol), K2CO3 (41.8 mg, 302 μmol), EtOH (1 ml) and water (0.3 ml). Oxygen was removed (high vacuum) and SilicaCat®Pd(0) (0.09 mmol/g loading; 112 mg, 10.1 μmol) was quickly added under nitrogen. The mixture was microwaved at 100° C. for 20 minutes, then concentrated. The material was redissolved in AcOH and purified by preparative HPLC to yield the title compound (12 mg; purity 95%). MS m/z [M+H]+ calc'd for C20H19ClN4O5, 431.10. found 431.4.

後処理

  1. stirringthe resulting mixture was stirred for 10 minutes
  2. customThe reaction mixture was evaporated under reduced pressure
  3. custompurified (C18 reverse phase column)
  4. additionwas quickly added under nitrogen
  5. customThe mixture was microwaved at 100° C. for 20 minutes
  6. concentrationconcentrated
  7. dissolutionThe material was redissolved in AcOH
  8. custompurified by preparative HPLC

出典と根拠

ORDレコード
ord-f4fde3c1484640edb4367232475e5349
出典データセット
uspto-grants-2015_09
特許番号
US09120747B2

反応ノート

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