N-methyl-2-pyrrolidone → rel-11-[(3R,4S)-3-fluoro-4-(hydroxymethyl)-4-methoxypiperidin-1-yl]-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamide

HRID 70798ノート

反応式

HRID 70798 の反応式
Cl.[F:2][C@H:3]1[C@:8]([CH2:11][OH:12])([O:9][CH3:10])[CH2:7][CH2:6][NH:5][CH2:4]1.CCN(C(C)C)C(C)C.CN1C(=O)CCC1.Cl[C:30]1[N:38]2[C:34](=[N:35][C:36]3[CH:42]=[CH:41][CH:40]=[CH:39][C:37]=32)[C:33]([C:43]([NH2:45])=[O:44])=[C:32]2[CH2:46][C:47]([CH3:50])([CH3:49])[CH2:48][C:31]=12>O>[F:2][C@H:3]1[C@:8]([CH2:11][OH:12])([O:9][CH3:10])[CH2:7][CH2:6][N:5]([C:30]2[N:38]3[C:34](=[N:35][C:36]4[CH:42]=[CH:41][CH:40]=[CH:39][C:37]=43)[C:33]([C:43]([NH2:45])=[O:44])=[C:32]3[CH2:46][C:47]([CH3:50])([CH3:49])[CH2:48][C:31]=23)[CH2:4]1

参加物

6

反応物 4

HCID 13387N-methyl-2-pyrrolidoneHCID 81531DiisopropylethylamineHCID 8941387611-chloro-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamideHCID 89413909rel-[(3R,4S)-3-fluoro-4-methoxypiperidin-4-yl]methanol hydrochloride

生成物 1

HCID 54588431rel-11-[(3R,4S)-3-fluoro-4-(hydroxymethyl)-4-methoxypiperidin-1-yl]-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamide収率 38.3%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

rel-[(3R,4S)-3-fluoro-4-methoxypiperidin-4-yl]methanol hydrochloride (399 mg) and DIPEA (523 μl) were added to an NMP (3 ml) solution of 11-chloro-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamide (314 mg), and heating and stirring were performed at 200° C. for 60 minutes under microwave irradiation. After adding water to the reaction liquid, the resulting precipitate was collected by filtration and dried under reduced pressure. The resulting solid was purified by silica gel column chromatography (MeOH/chloroform). The resulting crude purified matter was washed with chloroform-EtOAc-hexane to obtain rel-11-[(3R,4S)-3-fluoro-4-(hydroxymethyl)-4-methoxypiperidin-1-yl]-2,2-dimethyl-2,3-dihydro-1H-cyclopenta[4,5]pyrido[1,2-a]benzimidazole-4-carboxamide (169 mg).

後処理

  1. temperatureheating
  2. customwere performed at 200° C. for 60 minutes under microwave irradiation
  3. customto the reaction liquid
  4. filtrationthe resulting precipitate was collected by filtration
  5. customdried under reduced pressure
  6. customThe resulting solid was purified by silica gel column chromatography (MeOH/chloroform)
  7. customThe resulting crude purified matter
  8. washwas washed with chloroform-EtOAc-hexane

出典と根拠

ORDレコード
ord-2e9ce635640d40b0acc324e8d119694a
出典データセット
uspto-grants-2014_09
特許番号
US08822688B2

反応ノート

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