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Water → HCID 178523854、化合物

HRID 516458
ノート
印刷プレビュー

反応式

HRID 516458 の反応式
[OH:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[N:5]=[C:4]([C:13]([OH:15])=O)[CH:3]=1.CN(C(ON1N=NC2C=CC(=CC1=2)Cl)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CN(C=O)C.CC1OC(=O)OC=1C[O:54][C:55](=[O:75])[C@H:56]([OH:74])[CH2:57][C@H:58]([NH2:73])[CH2:59][C:60]1[CH:65]=[CH:64][C:63]([C:66]2[CH:71]=[CH:70][CH:69]=[C:68]([Cl:72])[CH:67]=2)=[CH:62][CH:61]=1.CCN(C(C)C)C(C)C.[Li+].[OH-].O>>[Cl:72][C:68]1[CH:67]=[C:66]([C:63]2[CH:62]=[CH:61][C:60]([CH2:59][C@@H:58]([NH:73][C:13]([C:4]3[CH:3]=[C:2]([OH:1])[N:6]([C:7]4[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=4)[N:5]=3)=[O:15])[CH2:57][C@@H:56]([OH:74])[C:55]([OH:75])=[O:54])=[CH:65][CH:64]=2)[CH:71]=[CH:70][CH:69]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 7

HCID 962WaterHCID 3939Lithium HydroxideHCID 6228DimethylformamideHCID 81531DiisopropylethylamineHCID 42624899O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphateHCID 86705143(2R,4R)-4-Amino-5-(3'-chlorobiphenyl-4-yl)-2-hydroxypentanoic acid 5-methyl-2-oxo[1,3]dioxol-4-ylmethyl ester
HCID 178524632
HCID 178524632、化合物

生成物 1

HCID 178523854HCID 178523854、化合物収率 58.4%

実験手順

5-Hydroxy-1-pyridin-2-yl-1H-pyrazole-3-carboxylic acid (59.0 mg, 287 μmol) and HCTU (131 mg, 316 μmol) were combined in DMF (1.3 mL, 17.2 mmol). and stirred at room temperature for 15 minutes. (2R,4R)-4-amino-5-(3′-chlorobiphenyl-4-yl)-2-hydroxypentanoic acid 5-methyl-2-oxo[1,3]dioxol-4-ylmethyl ester (100 mg, 0.3 mmol) and DIPEA (150 μL, 862 μmol) were added, and the resulting mixture was stirred at room temperature for 15 minutes. The reaction was evaporated under reduced pressure. The residue was dissolved in EtOH and a solution of 1 M LiOH in water (1.4 mL, 1.4 mmol) was added. The resulting mixture was stirred at room temperature for 1 hour, then evaporated under reduced pressure. The residue was purified by preparative HPLC to yield the title compound (85 mg). MS m/z [M+H]+ calc'd for C26H23ClN4O5, 507.14. found 507.1.

後処理

  1. stirringthe resulting mixture was stirred at room temperature for 15 minutes
  2. customThe reaction was evaporated under reduced pressure
  3. dissolutionThe residue was dissolved in EtOH
  4. stirringThe resulting mixture was stirred at room temperature for 1 hour
  5. customevaporated under reduced pressure
  6. customThe residue was purified by preparative HPLC

出典と根拠

ORDレコード
ord-ce0445d45c554fd1a3e844e7cd261934
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09108934B2

反応ノート

読み込み中…

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