Sodium Carbonate → 4-chloro-5-(4-phenoxyphenyl)-7-[1-(1-methyl-4-piperidinyl)-4-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidine

HRID 51617

反応式

HRID 51617 の反応式
N1C2NC=CC=2C=NC=1.[Cl:10][C:11]1[C:12]2[C:19](I)=[CH:18][N:17]([CH:21]3[CH2:26][CH2:25][N:24]([CH:27]4[CH2:32][CH2:31][N:30]([CH3:33])[CH2:29][CH2:28]4)[CH2:23][CH2:22]3)[C:13]=2[N:14]=[CH:15][N:16]=1.[O:34]([C:41]1[CH:46]=[CH:45][C:44](B(O)O)=[CH:43][CH:42]=1)[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1.C(=O)([O-])[O-].[Na+].[Na+]>COCCOC.O.C(#N)C>[Cl:10][C:11]1[C:12]2[C:19]([C:44]3[CH:45]=[CH:46][C:41]([O:34][C:35]4[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=4)=[CH:42][CH:43]=3)=[CH:18][N:17]([CH:21]3[CH2:26][CH2:25][N:24]([CH:27]4[CH2:32][CH2:31][N:30]([CH3:33])[CH2:29][CH2:28]4)[CH2:23][CH2:22]3)[C:13]=2[N:14]=[CH:15][N:16]=1

参加物

8

反応物 4

HCID 10340Sodium CarbonateHCID 2615917H-Pyrrolo(2,3-d)pyrimidineHCID 27343774-Phenoxyphenylboronic acidHCID 227361824-chloro-5-iodo-7-[1-(1-methyl-4-piperidinyl)-4-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidine

生成物 1

HCID 227362234-chloro-5-(4-phenoxyphenyl)-7-[1-(1-methyl-4-piperidinyl)-4-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidine収率 56.8%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 6342Acetonitrile溶媒HCID 80711,2-Dimethoxyethane溶媒

実験手順

1H NMR (DMSO-d6, 400 MHz) 8.62(s, 1H), 8.16(s, 1H), 4.66-4.58(m, 1H), 3.17(s, 1H), 3.02-3.00(d, 2H, J=8 Hz), 2.84-2.82 (d, 2H, J=8 Hz), 2.33-2.26(m, 2H), 2.17 (s, 3H), 2.08-2.04(m, 2H), 1.95-1.85 (m, 4H), 1.91-1.88(d, 2H, J=12 Hz), 1.49-1.45(m, 2H); Waters 2690 Alliance HPLC (Symmetry Shield RP18 3.5 μm, 2.1×50 mm; 5%-95% acetonitrile-0.1 M ammonium acetate over 15 min, 0.5 mL/min) Rt 3.505 min. 4-chloro-5-(4-phenoxyphenyl)-7-1-(1-methyl-4-piperidinyl)-4-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidine A mixture of 4-chloro-5-iodo-7-[ 1-(1-methyl-4-piperidinyl)-4-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidine (0.390 g, 0.845 mmol), 4-phenoxyphenyl boronic acid (0.199 g, 0.93 mmol), tetrakis(triphenylphosphine)pallidium (0.058 g, 0.051 mmol), and sodium carbonate (0.215 g, 2.03 mmol) were heated in a mixture of ethylene glycol dimethyl ether (20 mL) and water (10 mL) at 80° C. for 7 hours under a nitrogen atmosphere. Reaction solution was allowed to cool to room temperature, and the organic layer was removed under reduced pressure. Ethyl acetate was added, the layers were partitioned and the aqueous layer was extracted with ethyl acetate (250 mL). The organic layers were combined, washed with water and brine, dried over magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography on silica using 10% methanol in dichloromethane, then 20% methanol in dichloromethane as eluent to give 0.241 g (51%) of 4-chloro-5-(4-phenoxyphenyl)-7-[1-(1-methyl-4-piperidinyl)-4-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidine.

後処理

  1. customReaction solution
  2. customthe organic layer was removed under reduced pressure
  3. additionEthyl acetate was added
  4. customthe layers were partitioned
  5. extractionthe aqueous layer was extracted with ethyl acetate (250 mL)
  6. washwashed with water and brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. customevaporated under reduced pressure
  10. customThe residue was purified by flash chromatography on silica using 10% methanol in dichloromethane

出典と根拠

ORDレコード
ord-06863e454a6f4f95967bfc86066f1f47
出典データセット
uspto-grants-2004_03
特許番号
US06713474B2

関連ノート

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