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Diisopropylethylamine → HCID 44540686、化合物

HRID 1616004
ノート
印刷プレビュー

反応式

HRID 1616004 の反応式
[CH3:1][N:2]([CH2:4][C:5]1[N:10]=[C:9]([C:11]([OH:13])=O)[CH:8]=[CH:7][CH:6]=1)[CH3:3].F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.CCN(C(C)C)C(C)C.[NH:47]1[C:55]2[C:50](=[C:51]([C:56]3[CH:57]=[C:58]([NH2:71])[C:59]4[C:63]([CH:64]=3)=[N:62][N:61](C3CCCCO3)[CH:60]=4)[CH:52]=[CH:53][CH:54]=2)[CH:49]=[CH:48]1.C(=O)(O)[O-].[Na+]>CN(C=O)C>[CH3:3][N:2]([CH2:4][C:5]1[N:10]=[C:9]([C:11]([NH:71][C:58]2[CH:57]=[C:56]([C:51]3[CH:52]=[CH:53][CH:54]=[C:55]4[C:50]=3[CH:49]=[CH:48][NH:47]4)[CH:64]=[C:63]3[C:59]=2[CH:60]=[N:61][NH:62]3)=[O:13])[CH:8]=[CH:7][CH:6]=1)[CH3:1]
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 81531DiisopropylethylamineHCID 516892Sodium BicarbonateHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 582679956-(1H-Indol-4-yl)-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-4-amineHCID 58268028HCID 58268028、化合物

生成物 1

HCID 44540686
HCID 44540686、化合物
収率 53.6%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A solution of 6-[(dimethylamino)methyl]-2-pyridinecarboxylic acid (27 mg, 0.15 mmol) in DMF (0.0008 ml) was treated with O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (72 mg, 0.19 mmol) and DIPEA (0.052 ml). After 5 minutes the resulting solution was added to 6-(1H-indol-4-yl)-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-4-amine (33 mg, 0.10 mmol). After stirring for 90 mins at room temperature the mixture was treated with saturated sodium bicarbonate solution (10 ml) and extracted with dichloromethane (3×10 ml). The extracts were passed through a hydrophobic frit, combined and the solvent was evaporated under nitrogen flow. The residue was dissolved in methanol (2 ml) and hydrochloric acid (2M, 0.080 ml) was added. The solvents were evaporated under nitrogen stream to give a crude product which was purified by Mass Directed Automated Preparative HPLC (Method B). Fractions containing pure product were evaporated under a nitrogen stream to give the title compound (22 mg) as a pale solid.

後処理

  1. extractionextracted with dichloromethane (3×10 ml)
  2. customthe solvent was evaporated under nitrogen flow
  3. dissolutionThe residue was dissolved in methanol (2 ml)
  4. additionhydrochloric acid (2M, 0.080 ml) was added
  5. customThe solvents were evaporated under nitrogen stream
  6. customto give a crude product which
  7. customwas purified by Mass Directed Automated Preparative HPLC (Method B)
  8. additionFractions containing pure product
  9. customwere evaporated under a nitrogen stream

出典と根拠

ORDレコード
ord-f0625fe98fe243f1a9901c7254e8246a
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08765743B2

反応ノート

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