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Piperidine → 3-Amino-oxetane-3-carboxylic acid {(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-yl}-amide

HRID 2046598
ノート
印刷プレビュー

反応式

HRID 2046598 の反応式
C1C2C(COC(=O)[NH:17][C:18]3([C:22](=[O:47])[NH:23][C@@H:24]4[C:32]5[C:27](=[CH:28][C:29]([C:33]6[CH:38]=[C:37]([Cl:39])[CH:36]=[C:35]([F:40])[C:34]=6[C:41]6[N:45]=[C:44]([CH3:46])[O:43][N:42]=6)=[CH:30][CH:31]=5)[CH2:26][CH2:25]4)[CH2:21][O:20][CH2:19]3)C3C(=CC=CC=3)C=2C=CC=1.N1CCCCC1>C(Cl)Cl>[Cl:39][C:37]1[CH:36]=[C:35]([F:40])[C:34]([C:41]2[N:45]=[C:44]([CH3:46])[O:43][N:42]=2)=[C:33]([C:29]2[CH:28]=[C:27]3[C:32](=[CH:31][CH:30]=2)[C@@H:24]([NH:23][C:22]([C:18]2([NH2:17])[CH2:19][O:20][CH2:21]2)=[O:47])[CH2:25][CH2:26]3)[CH:38]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 8082PiperidineHCID 68296802(3-{(S)-5-[5-Chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-ylcarbamoyl}-oxetan-3-yl)-carbamic acid 9H-fluoren-9-ylmethyl ester

生成物 1

HCID 601410403-Amino-oxetane-3-carboxylic acid {(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-yl}-amide

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of (3-{(S)-5-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-indan-1-ylcarbamoyl}-oxetan-3-yl)-carbamic acid 9H-fluoren-9-ylmethyl ester (intermediate A-12) (2.94 g, 4.42 mmol) in MeCl2 (50.0 ml) was added piperidine (4.38 ml) and the mixture was stirred at room temperature for 15 h. The colorless solution was concentrated to dryness under high vacuum at RT. The remaining residue was purified by chromatography (silica gel; MeCl2/MeOH 100:0-95:5) and the title compound was obtained as light brown oil (1.09 g, 56%). MS: 443.1 (MH+, 1Cl).

後処理

  1. concentrationThe colorless solution was concentrated to dryness under high vacuum at RT
  2. customThe remaining residue was purified by chromatography (silica gel; MeCl2/MeOH 100:0-95:5)

出典と根拠

ORDレコード
ord-fe591d7b037b415197032ccb6fc07c31
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08592426B2

反応ノート

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