Acetic Acid → 5-{4-[4-((2S)-2-Hydroxy-3-phenoxy-propylamino)-piperidin-1-yl]-benzylidene}-2-thioxo-thiazolidin-4-one

HRID 1794742ノート

反応式

HRID 1794742 の反応式
[O:1]=[C:2]1[C:6](=[CH:7][C:8]2[CH:13]=[CH:12][C:11]([N:14]3[CH2:19][CH2:18][C:17](=O)[CH2:16][CH2:15]3)=[CH:10][CH:9]=2)[S:5][C:4](=[S:21])[NH:3]1.[NH2:22][CH2:23][C@H:24]([OH:33])[CH2:25][O:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(O)(=O)C>ClCCCl>[OH:33][C@H:24]([CH2:25][O:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[CH2:23][NH:22][CH:17]1[CH2:18][CH2:19][N:14]([C:11]2[CH:12]=[CH:13][C:8]([CH:7]=[C:6]3[S:5][C:4](=[S:21])[NH:3][C:2]3=[O:1])=[CH:9][CH:10]=2)[CH2:15][CH2:16]1

参加物

6

反応物 4

HCID 176Acetic AcidHCID 1133101(2S)-(-)-1-Amino-3-phenoxy-2-propanolHCID 5049666Sodium triacetoxyborohydrideHCID 731782011-[4-(4-Oxo-2-thioxo-thiazolidin-5-ylidenemethyl)-phenyl]-piperidin-4-one

生成物 1

HCID 865845495-{4-[4-((2S)-2-Hydroxy-3-phenoxy-propylamino)-piperidin-1-yl]-benzylidene}-2-thioxo-thiazolidin-4-one

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

1-[4-(4-Oxo-2-thioxo-thiazolidin-5-ylidenemethyl)-phenyl]-piperidin-4-one (which was obtained in Example 34) (0.16 g, 0.5 mmol) and (2S)-1-amino-3-phenoxy-propan-2-ol (which was obtained in Example 3) (0.12 g, 0.75 mmol) were mixed in 1,2-dichloroethane (10 mL) and then treated with sodium triacetoxyborohydride (0.16 g, 0.75 mmol) and acetic acid (0.045 g, 0.75 mmol). After stirring at room temperature under a nitrogen atmosphere for one day the mixture was quenched with 1N sodium hydroxide (NaOH) and then poured into a saturated aqueous sodium bicarbonate (NaHCO3). The aqueous layer was extracted with dichloromethane and the combined organic layers were dried and concentrated. The residue was purified by preparative thin layer chromatography (16% MeOH/CH2CH2) to give the title compound as a pale yellowish solid; mp>220° C. (decomposed); 1H NMR (300 MHz, DMSO-d6) δ 1.50–1.70 (m, 2 H), 1.90–2.10 (m, 2 H), 2.60–3.40 (m, 7 H), 3.90–4.20 (m, 3 H), 6.70–7.15 (m, 6 H), 7.30 (d, J=8.8 Hz, 2 H); 7.38 (d, J=8.8 Hz, 2 H); MS (ES) m/z: 470.0 (MH+); HRMS Calcd. for C24H27N3O3S2(M+): 469.1494. Found: 469.1488.

後処理

  1. customwas quenched with 1N sodium hydroxide (NaOH)
  2. additionpoured into a saturated aqueous sodium bicarbonate (NaHCO3)
  3. extractionThe aqueous layer was extracted with dichloromethane
  4. customthe combined organic layers were dried
  5. concentrationconcentrated
  6. customThe residue was purified by preparative thin layer chromatography (16% MeOH/CH2CH2)

出典と根拠

ORDレコード
ord-1f23f5841d6242c7af05b039966285a3
出典データセット
uspto-grants-2006_04
特許番号
US07022716B2

反応ノート

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