Diisopropylethylamine → N2-acetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl) guanosine

HRID 1694676

反応式

HRID 1694676 の反応式
[C:1]([NH:4][C:5]1[NH:6][C:7](=[O:46])[C:8]2[N:9]=[CH:10][N:11]([C:44]=2[N:45]=1)[C@@H:12]1[O:43][C@H:17]([CH2:18][O:19][C:20]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)([C:29]2[CH:34]=[CH:33][C:32]([O:35][CH3:36])=[CH:31][CH:30]=2)[C:21]2[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[CH:23][CH:22]=2)[C@@H:15]([OH:16])[C@H:13]1[OH:14])(=[O:3])[CH3:2].C(N(C(C)C)CC)(C)C.[C:56]([CH2:58][CH2:59][O:60][CH2:61]Cl)#[N:57].C(=O)(O)[O-].[Na+]>ClCCCl>[C:1]([NH:4][C:5]1[NH:6][C:7](=[O:46])[C:8]2[N:9]=[CH:10][N:11]([C:44]=2[N:45]=1)[C@@H:12]1[O:43][C@H:17]([CH2:18][O:19][C:20]([C:37]2[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=2)([C:29]2[CH:34]=[CH:33][C:32]([O:35][CH3:36])=[CH:31][CH:30]=2)[C:21]2[CH:22]=[CH:23][C:24]([O:27][CH3:28])=[CH:25][CH:26]=2)[C@@H:15]([OH:16])[C@H:13]1[O:14][CH2:61][O:60][CH2:59][CH2:58][C:56]#[N:57])(=[O:3])[CH3:2]

参加物

6

反応物 4

HCID 81531DiisopropylethylamineHCID 516892Sodium BicarbonateHCID 116654052-Cyanoethyl chloromethyl etherHCID 136122477N-Acetyl-5'-DMTguanosine

生成物 1

HCID 136387249N2-acetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl) guanosine収率 63.3%

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

N2-Acetyl-5′-O-(4,4′-dimethoxytrityl)guanosine (627 mg, 1 mmol) was dissolved in 4 mL of 1,2-dichloroethane, and 452 mg of diisopropylethylamine (3.5 mmol) was added, and then 365 mg of dibutylstannyl dichloride (1.2 mmol) was added. And then, the reaction solution was reacted at room temperature for 1 hour. Then, the reaction was performed at 80° C., and 155.4 mg of chloromethyl 2-cyanoethyl ether (1.3 mmol) was added dropwise, and the solution was stirred for 60 minutes. After the reaction completed, the reaction solution was mixed with an aqueous saturated sodium bicarbonate solution, and was subjected to extraction with methylene chloride. The extract was dried over anhydrous magnesium sulfate, and the solvent was distilled off. The obtained mixture was purified by 30 g of silica gel column chromatography to obtain N2-acetyl-5′-O-(4,4′-dimethoxytrityl)-2′-O-(2-cyanoethoxymethyl) guanosine (450 mg, yield 63%).

後処理

  1. customAnd then, the reaction solution was reacted at room temperature for 1 hour
  2. customwas performed at 80° C.
  3. extractionwas subjected to extraction with methylene chloride
  4. dry with materialThe extract was dried over anhydrous magnesium sulfate
  5. distillationthe solvent was distilled off
  6. customThe obtained mixture was purified by 30 g of silica gel column chromatography

出典と根拠

ORDレコード
ord-fd7d1f7ef1304c92abc5b4f55a5e26f0
出典データセット
uspto-grants-2012_04
特許番号
US08158775B2

関連ノート

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