Tributylamine → (2S)-N,2-dimethyl-2-{methyl[(4-{(E)-2-[4-(morpholin-4-ylmethyl)phenyl]ethenyl}phenyl)carbonyl]amino}-N'-(tetrahydro-2H-pyran-2-yloxy)propanediamide

HRID 1519739ノート

反応式

HRID 1519739 の反応式
CC1C=CC(P([C:16]2[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=2)C2C=CC(C)=CC=2)=CC=1.[CH2:23](N(CCCC)CCCC)[CH2:24]CC.I[C:37]1[CH:62]=[CH:61][C:40]([C:41]([N:43]([CH3:60])[C@:44]([CH3:59])([C:49]([NH:51][O:52][CH:53]2[CH2:58][CH2:57][CH2:56][CH2:55][O:54]2)=[O:50])[C:45]([NH:47][CH3:48])=[O:46])=[O:42])=[CH:39][CH:38]=1.C(C1C=CC(C=O)=CC=1)=C.[NH:73]1[CH2:78][CH2:77][O:76][CH2:75][CH2:74]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)([O-])O.[Na+]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C(Cl)(Cl)Cl.C(O)(=O)C.CN(C=O)C>[CH3:48][NH:47][C:45](=[O:46])[C@:44]([CH3:59])([N:43]([CH3:60])[C:41]([C:40]1[CH:61]=[CH:62][C:37](/[CH:23]=[CH:24]/[C:16]2[CH:17]=[CH:18][C:19]([CH2:22][N:73]3[CH2:78][CH2:77][O:76][CH2:75][CH2:74]3)=[CH:20][CH:21]=2)=[CH:38][CH:39]=1)=[O:42])[C:49]([NH:51][O:52][CH:53]1[CH2:58][CH2:57][CH2:56][CH2:55][O:54]1)=[O:50]

参加物

12

反応物 7

HCID 7622TributylamineHCID 8083MorpholineHCID 13956Phosphine, tris(4-methylphenyl)-HCID 393894-VinylbenzaldehydeHCID 516892Sodium BicarbonateHCID 5049666Sodium triacetoxyborohydrideHCID 86679252HCID 86679252、化合物2 回

生成物 1

HCID 86679298(2S)-N,2-dimethyl-2-{methyl[(4-{(E)-2-[4-(morpholin-4-ylmethyl)phenyl]ethenyl}phenyl)carbonyl]amino}-N'-(tetrahydro-2H-pyran-2-yloxy)propanediamide収率 31%

試薬・触媒・溶媒 4

HCID 167845palladium(II) acetate触媒HCID 176Acetic Acid溶媒HCID 6212Chloroform溶媒HCID 6228Dimethylformamide溶媒

反応条件

温度
80 °C

実験手順

Palladium acetate (12 mg), tris(4-methylphenyl)phosphine (24 mg), tri-n-butylamine (0.25 mL) were added to a DMF (1.2 ml) solution of (2S)-2-[(4-iodobenzoyl)(methyl)amino]-N,2-dimethyl-N′-(tetrahydro-2H-pyran-2-yloxy)propanediamide (Intermediate 15, 90 mg) and 4-ethenylbenzaldehyde (98 mg) obtained by the same method as the synthesis method described in the literature (Journal of Electroanalytical Chemistry, 2002, Vol. 529(1), pp. 43-50), and the mixture was stirred overnight at 80° C. The solvent was distilled off under reduced pressure, and the resulting residue was purified by OH type silica gel chromatography (gradient elution with chloroform/methanol=100/0→94/6) to obtain a crude product. Morpholine (30 μl) and acetic acid (20 μl) were added to a chloroform (1.0 ml) solution of the resulting crude product, and the mixture was stirred for 2.5 hours at room temperature. Further, sodium triacetoxyborohydride (62 mg) was added, and the mixture was stirred overnight at room temperature. A saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture, the mixture was extracted with chloroform, and the organic layer was concentrated under reduced pressure. The resulting residue was purified by NH type silica gel chromatography (gradient elution with chloroform/methanol=100/0→94/6) to obtain (2S)-N,2-dimethyl-2-{methyl[(4-{(E)-2-[4-(morpholin-4-ylmethyl)phenyl]ethenyl}phenyl)carbonyl]amino}-N′-(tetrahydro-2H-pyran-2-yloxy)propanediamide (colorless oil) (32 mg, 31%).

後処理

  1. customobtained by the same method as the synthesis method
  2. distillationThe solvent was distilled off under reduced pressure
  3. customthe resulting residue was purified by OH type silica gel chromatography (gradient elution with chloroform/methanol=100/0→94/6)
  4. customto obtain a crude product
  5. stirringthe mixture was stirred for 2.5 hours at room temperature
  6. stirringthe mixture was stirred overnight at room temperature
  7. extractionthe mixture was extracted with chloroform
  8. concentrationthe organic layer was concentrated under reduced pressure
  9. customThe resulting residue was purified by NH type silica gel chromatography (gradient elution with chloroform/methanol=100/0→94/6)

出典と根拠

ORDレコード
ord-025720124c114304ac4343138e97ef4d
出典データセット
uspto-grants-2015_07
特許番号
US09073821B2

反応ノート

読み込み中…