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Sodium borohydride → 6-Bis(phenylmethyl)amino-4,5-diamino-pyridine-3-carboxylic acid ethyl ester

HRID 1268833
ノート
印刷プレビュー

反応式

HRID 1268833 の反応式
[BH4-].[Na+].[CH2:3]([O:5][C:6]([C:8]1[CH:9]=[N:10][C:11]([N:18]([CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)[CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[C:12]([N+:15]([O-])=O)[C:13]=1[NH2:14])=[O:7])[CH3:4]>CO.ClCCl.O.[Ni](Cl)Cl>[CH2:3]([O:5][C:6]([C:8]1[CH:9]=[N:10][C:11]([N:18]([CH2:26][C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=2)[CH2:19][C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)=[C:12]([NH2:15])[C:13]=1[NH2:14])=[O:7])[CH3:4]
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 2

HCID 4311764Sodium borohydride2 回HCID 690647034-Amino-6-bis(phenylmethyl)amino-5-nitro-pyridine-3-carboxylic acid ethyl ester

生成物 1

HCID 690704746-Bis(phenylmethyl)amino-4,5-diamino-pyridine-3-carboxylic acid ethyl ester収率 24.1%

試薬・触媒・溶媒 3

HCID 16212333Nickel chloride hydrate触媒HCID 887Methanol
溶媒
HCID 6344Dichloromethane溶媒

実験手順

Sodium borohydride (151 mg, 4.1 mmol) was added to a solution of nickel (II) chloride hydrate (261 mg, 1.1 mmol) in MeOH (26 mL). After 30 min. at room temperature, a solution of 4-amino-6-bis(phenylmethyl)amino-5-nitro-pyridine-3-carboxylic acid ethyl ester (0.9 g, 2.2 mmol) in dichloromethane (5 mL) was added followed by the addition of sodium borohydride (353 mg). The mixture was stirred over night then filtered through a layer of silica gel. The organic was diluted with dichloromethane, washed with brine and dried over sodium sulfate. The organics were filtered, concentrated and purified by column chromatography (dichloromethane:methanol, 20:1). 11 was obtained as a white solid (200 mg). 1H NMR (400 MHz, d6-DMSO) δ: 1.26 (t, J=7.1 Hz, 3H), 4.21 (s, 4H), 4.22 (q, J=7.1 Hz, 2H), 4.52 (s, 2H), 6.73 (s, 2H), 7.14–7.31 (m, 10H), 8.01 (s, 1H). ESIMS, M/Z, 377 (M+1)+.

後処理

  1. filtrationthen filtered through a layer of silica gel
  2. additionThe organic was diluted with dichloromethane
  3. washwashed with brine
  4. dry with materialdried over sodium sulfate
  5. filtrationThe organics were filtered
  6. concentrationconcentrated
  7. custompurified by column chromatography (dichloromethane:methanol, 20:1)

出典と根拠

ORDレコード
ord-22383ad2578a4a9cbeb39c3c72ee2280
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07199119B2

反応ノート

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