ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

1-Hydroxybenzotriazole → Tert-Butyl 6-{[2-cyclopentyl-2-{4-[(5-oxo-2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-4-yl)-methyl]phenyl}acetyl]amino}heptanoate

HRID 238185
ノート
印刷プレビュー

反応式

HRID 238185 の反応式
[CH:1]1[CH:2]=[CH:3][C:4]2N(O)N=N[C:5]=2[CH:6]=1.CCN(C(C)C)C(C)C.[CH:20]1([CH:25]([C:29]2[CH:34]=[CH:33][C:32]([CH2:35][N:36]3[C:41](=[O:42])[CH2:40][O:39][C:38](C4C=CC=CC=4)=[N:37]3)=[CH:31][CH:30]=2)[C:26]([OH:28])=O)[CH2:24][CH2:23][CH2:22][CH2:21]1.[NH2:49][CH:50]([CH3:62])[CH2:51][CH2:52][CH2:53][CH2:54][C:55]([O:57][C:58]([CH3:61])([CH3:60])[CH3:59])=[O:56].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>CN(C=O)C.C(OCC)(=O)C>[CH:20]1([CH:25]([C:29]2[CH:30]=[CH:31][C:32]([CH2:35][N:36]3[C:41](=[O:42])[CH2:40][O:39][C:38]([C:5]4[CH:4]=[CH:3][CH:2]=[CH:1][CH:6]=4)=[N:37]3)=[CH:33][CH:34]=2)[C:26]([NH:49][CH:50]([CH3:62])[CH2:51][CH2:52][CH2:53][CH2:54][C:55]([O:57][C:58]([CH3:61])([CH3:60])[CH3:59])=[O:56])=[O:28])[CH2:24][CH2:23][CH2:22][CH2:21]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 13997370Tert-butyl 6-aminoheptanoateHCID 58074507cyclopentyl{4-[(5-oxo-2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-4-yl)methyl]phenyl}acetic acid

生成物 1

HCID 58074539
Tert-Butyl 6-{[2-cyclopentyl-2-{4-[(5-oxo-2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-4-yl)-methyl]phenyl}acetyl]amino}heptanoate

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
0 °C

実験手順

At RT, 41.3 mg (0.306 mmol) of HOBt and 126 μl (0.764 mmol) of DIEA were added to a solution of 100 mg (0.255 mmol) of (+)-cyclopentyl{4-[(5-oxo-2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-4-yl)methyl]phenyl}acetic acid and 76.9 mg (0.382 mmol) of tert-butyl(+/−)-6-aminoheptanoate in 0.3 ml of DMF. The resulting mixture was cooled to 0° C., after which 116.3 mg (0.306 mmol) of HATU were added. The reaction mixture was slowly warmed to RT, stirred at RT for 1 h and then diluted with ethyl acetate. The organic phase was washed with saturated sodium bicarbonate solution and with saturated sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by preparative RP-HPLC (acetonitrile/water gradient). This gave 118 mg (about 83% pure, about 67% of theory) of the target compound as a diastereomer mixture.

後処理

  1. temperatureThe reaction mixture was slowly warmed to RT
  2. washThe organic phase was washed with saturated sodium bicarbonate solution and with saturated sodium chloride solution
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by preparative RP-HPLC (acetonitrile/water gradient)

出典と根拠

ORDレコード
ord-4b9e794f2e9e4f5c9f4019ec50ee243d
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08642592B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート