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4-Methylmorpholine → HCID 44156014、化合物

HRID 572627
ノート
印刷プレビュー

反応式

HRID 572627 の反応式
[C:1]([C:3]1[C:4]([C:17]2[CH:22]=[CH:21][C:20]([Cl:23])=[C:19]([Cl:24])[CH:18]=2)=[C:5]([C:14]([OH:16])=O)[S:6][C:7]=1[N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1)#[N:2].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CN1CCOCC1.[CH3:56][N:57]1[C:61]([NH2:62])=[CH:60][C:59]([CH3:63])=[N:58]1>CN(C=O)C>[C:1]([C:3]1[C:4]([C:17]2[CH:22]=[CH:21][C:20]([Cl:23])=[C:19]([Cl:24])[CH:18]=2)=[C:5]([C:14]([NH:62][C:61]2[N:57]([CH3:56])[N:58]=[C:59]([CH3:63])[CH:60]=2)=[O:16])[S:6][C:7]=1[N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1)#[N:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 79724-MethylmorpholineHCID 5207211,3-Dimethyl-1H-pyrazol-5-amineHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 441558954-Cyano-3-(3,4-dichlorophenyl)-5-morpholin-4-ylthiophene-2-carboxylic acid

生成物 1

HCID 44156014HCID 44156014、化合物収率 10%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

4-cyano-3-(3,4-dichlorophenyl)-5-morpholin-4-ylthiophene-2-carboxylic acid (0.030 g, 0.07 mmol), HBTU (0.080 g, 0.21 mmol), N-methyl morpholine (0.023 mL, 0.21 mmol) and DMF (1 mL) were added to a sealed reaction tube containing 1,3-dimethyl-1H-pyrazol-5-amine (0.023 g, 0.21 mmol). The reaction mixture was allowed to shake overnight and was concentrated. The residue was dissolved up in THF/chloroform (1:3) (4 mL) and washed with sat NaHCO3 (2 mL). The organic solution was separated and concentrated. The crude product was dissolved in DMSO (1.5 mL) and was purified by reverse phase chromatography to give 4-cyano-3-(3,4-dichlorophenyl)-N-(1,3-dimethyl-1H-pyrazol-5-yl)-5-morpholin-4-ylthiophene-2-carboxamide (85) (0.003 g, 10%). LCMS: (FA) ES+ 476.4.

後処理

  1. concentrationwas concentrated
  2. dissolutionThe residue was dissolved up in THF/chloroform (1:3) (4 mL)
  3. washwashed
  4. customThe organic solution was separated
  5. concentrationconcentrated
  6. dissolutionThe crude product was dissolved in DMSO (1.5 mL)
  7. customwas purified by reverse phase chromatography

出典と根拠

ORDレコード
ord-c81ab7cfe17847249b094d835e7dfec1
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09029411B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート