Triphenylphosphine → (1r)-Cyclopropanecarboxylic acid {2-[1-(3-ethoxy-4-methoxy-phenyl)-3-methanesulfonyl-propyl]-3-oxo-2,3-dihydro-1h-isoindol-4-yl}-amide

HRID 1797236ノート

反応式

HRID 1797236 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C.[CH2:34]([O:36][C:37]1[CH:38]=[C:39]([C@H:45]([N:49]2[C:57](=[O:58])[C:56]3[C:51](=[CH:52][CH:53]=[CH:54][C:55]=3[NH:59][C:60]([CH:62]3[CH2:64][CH2:63]3)=[O:61])[CH2:50]2)[CH2:46][CH2:47]O)[CH:40]=[CH:41][C:42]=1[O:43][CH3:44])[CH3:35].[CH3:65][S-].[Na+].O[O:69][S:70]([O-:72])=O.[K+]>C1COCC1.CO.O>[CH2:34]([O:36][C:37]1[CH:38]=[C:39]([C@H:45]([N:49]2[C:57](=[O:58])[C:56]3[C:51](=[CH:52][CH:53]=[CH:54][C:55]=3[NH:59][C:60]([CH:62]3[CH2:64][CH2:63]3)=[O:61])[CH2:50]2)[CH2:46][CH2:47][S:70]([CH3:65])(=[O:72])=[O:69])[CH:40]=[CH:41][C:42]=1[O:43][CH3:44])[CH3:35]

参加物

9

反応物 5

HCID 11776TriphenylphosphineHCID 4378561Sodium methanethiolateHCID 5363146Diisopropyl azodicarboxylateHCID 9845251(1R)-cyclopropanecarboxylic acid {2-[1-(3-ethoxy-4-methoxy-phenyl)-3-hydroxy-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amideHCID 23707502Potassium hydroxy sulfite

生成物 1

HCID 10413135(1r)-Cyclopropanecarboxylic acid {2-[1-(3-ethoxy-4-methoxy-phenyl)-3-methanesulfonyl-propyl]-3-oxo-2,3-dihydro-1h-isoindol-4-yl}-amide収率 5%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of triphenyl phosphine (0.63 g, 2.4 mmol) in THF (10 mL) was added DIAD (0.47 mL, 2.4 mmol) at 0° C. After 10 min, (1R)-cyclopropanecarboxylic acid {2-[1-(3-ethoxy-4-methoxy-phenyl)-3-hydroxy-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide (0.93 mL, 2.2 mmol) was added as solid. After 5 min, sodium thiomethoxide (180 mg, 2.6 mmol) was added. After 20 min, the cold bath was removed and the mixture was stirred at room temperature for 1.5 hrs. To the mixture was added water (15 mL), methanol (15 mL), and oxone (5.4 g, 8.8 mmol) and kept for 16 h. The mixture was extracted with methylene chloride (100 mL) and water (50 mL). The organic layer was dried over MgSO4. The solvent was removed in vacuo to give a solid. The solid was purified with prep HPLC to give (1R)-cyclopropanecarboxylic acid {2-[1-(3-ethoxy-4-methoxy-phenyl)-3-methanesulfonyl-propyl]-3-oxo-2,3-dihydro-1H-isoindol-4-yl}-amide as a white solid (50 mg, 5% yield): mp, 148–150° C.; 1H NMR (CDCl3) δ 0.89–0.94 (m, 2H, CH2), 1.10–1.13 (m, 2H, CH2), 1.46 (t, J=7 Hz, 3H, CH3), 1.65–1.73 (m, 1H, CH), 2.60–2.69 (m, 2H, CH2), 2.96 (s, 3H, CH3), 3.02–3.22 (m, 2H, CH2), 3.87 (s, 3H, CH3), 3.99 (d, J=17 Hz, 1H, NCHH), 4.07 (q, J=7 Hz, 2H, CH2), 4.30 (d, J=17 Hz, 1H, NCHH), 5.48 (t, J=8 Hz, 1H, NCH), 6.84–7.02 (m, 4H, Ar), 7.46 (t, J=8 Hz, 1H, Ar), 8.45 (d, J=8 Hz, 1H, Ar), 10.49 (s, 1H, NH); 13C NMR (CDCl3) δ 8.30, 14.75, 16.19, 23.78, 41.24, 45.95, 51.99, 53.01, 56.00, 64.65, 111.60, 112.37, 116.88, 117.00, 117.89, 119.46, 129.82, 133.52, 138.09, 141.29, 148.87, 149.55, 169.79, 172.66; Anal Calcd for C25H30N2O6S1: C, 61.71; H, 6.21; N, 5.76. Found: C, 61.33; H, 6.19; N, 5.59.

後処理

  1. waitAfter 5 min
  2. waitAfter 20 min
  3. customthe cold bath was removed
  4. waitkept for 16 h
  5. extractionThe mixture was extracted with methylene chloride (100 mL) and water (50 mL)
  6. dry with materialThe organic layer was dried over MgSO4
  7. customThe solvent was removed in vacuo
  8. customto give a solid
  9. customThe solid was purified with prep HPLC

出典と根拠

ORDレコード
ord-1bc993bd044c43828823666da153d5d3
出典データセット
uspto-grants-2006_04
特許番号
US07034052B2

反応ノート

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