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Pyridine → HCID 57741115、化合物

HRID 1092433
ノート
印刷プレビュー

反応式

HRID 1092433 の反応式
[CH3:1][C:2]([O:4][C:5]([CH3:7])=[O:6])=O.[Cl:8][C:9]1[CH:14]=[CH:13][C:12]([C@@H:15]2[C@@H:20]([OH:21])[C@H](CO)[C@@H:18]([OH:24])[C@H:17]([OH:25])[C@H:16]2[OH:26])=[CH:11][C:10]=1[CH2:27][C:28]1[CH:33]=[CH:32][C:31]([CH2:34][CH3:35])=[CH:30][CH:29]=1.N1C=CC=CC=1>CN(C1C=CN=CC=1)C.C(Cl)Cl>[C:5]([O:4][CH2:2][C@@H:1]1[C@@H:18]([OH:24])[C@H:17]([OH:25])[C@@H:16]([OH:26])[C@H:15]([C:12]2[CH:13]=[CH:14][C:9]([Cl:8])=[C:10]([CH2:27][C:28]3[CH:29]=[CH:30][C:31]([CH2:34][CH3:35])=[CH:32][CH:33]=3)[CH:11]=2)[C@H:20]1[OH:21])(=[O:6])[CH3:7]
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 3

HCID 1049PyridineHCID 7918Acetic AnhydrideHCID 42622954HCID 42622954、化合物

生成物 1

HCID 57741115HCID 57741115、化合物収率 50.4%

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane溶媒

実験手順

Ac2O (377 mg, 1.5 eq) was added dropwised into the solution of (1R,2R,3S,4R,5R,6S)-4-(4-chloro-3-(4-ethylbenzyl)phenyl)-6-(hydroxymethyl)cyclohexane-1,2,3,5-tetraol (5, R=Et, 1 g, 2.46 mmol) and DMAP (cat.) in CH2Cl2 (10 mL) at 0° C. followed by pyridine (292 mg, 1.5 eq), and the mixture was stirred overnight at rt. The reaction mixture was washed with 3N HCl, and the organic layer was combined, dried over Na2SO4, filtered, and the filtrate was evaporated to dryness. The residue was purified by preperative HPLC to give target compound (566 mg, white solid, yield of 50.4%). 1H-NMR (400 MHz, CD3OD): δ 7.32 (1H, d, J=8.4 Hz), 7.06-7.14 (6H, m), 4.37 (2H, ddd, J=2.0, 10.8, 16.8 Hz), 4.04 (2H, s), 3.57 (1H, t, J=10.8 Hz), 3.40-3.47 (1H, m), 2.49-2.60 (3H, m), 2.04 (3H, s), 1.60-1.66 (1H, m), 1.18 (3H, t, J=8.0 Hz); MS (ESI+): 449 [M+H]+, 466 [M+NH4]+, 897 [2M+H]+, (ESI−): 492 [M+HCOO]−, 941 [2M+HCOO]−.

後処理

  1. washThe reaction mixture was washed with 3N HCl
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. customthe filtrate was evaporated to dryness
  5. customThe residue was purified by preperative HPLC
  6. customto give target compound (566 mg, white solid, yield of 50.4%)

出典と根拠

ORDレコード
ord-3f9fbf09a3e54d60a677210f2d85d9f6
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08129434B2

反応ノート

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