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1,4-Dihydro-2,6-dimethyl-4-(3-isothiocyanatophenyl)-3,5-pyrazinedicarboxylic acid, dimethyl ester → HCID 178498419、化合物

HRID 566904
ノート
印刷プレビュー

反応式

HRID 566904 の反応式
[CH3:1][C:2]1[NH:3][C:4]([CH3:25])=[C:5]([C:21]([O:23][CH3:24])=[O:22])[N:6]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([N:18]=[C:19]=S)[CH:13]=2)[C:7]=1[C:8]([O:10][CH3:11])=[O:9].[N:26]#[C:27][NH2:28].[Na].[C:30]1([CH:36]2[CH2:41][CH2:40][N:39]([CH2:42][CH2:43][CH2:44][NH2:45])[CH2:38][CH2:37]2)[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>CCO.C1COCC1.Cl[Hg]Cl>[C:27]([N:28]=[C:19]([NH:18][C:14]1[CH:13]=[C:12]([N:6]2[C:7]([C:8]([O:10][CH3:11])=[O:9])=[C:2]([CH3:1])[NH:3][C:4]([CH3:25])=[C:5]2[C:21]([O:23][CH3:24])=[O:22])[CH:17]=[CH:16][CH:15]=1)[NH:45][CH2:44][CH2:43][CH2:42][N:39]1[CH2:38][CH2:37][CH:36]([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[CH2:41][CH2:40]1)#[N:26]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 155242381,4-Dihydro-2,6-dimethyl-4-(3-isothiocyanatophenyl)-3,5-pyrazinedicarboxylic acid, dimethyl esterHCID 22725156HCID 22725156、化合物HCID 57375518Cyanamidnatrium

生成物 1

HCID 178498419HCID 178498419、化合物

試薬・触媒・溶媒 3

HCID 24085Mercuric Chloride触媒
HCID 702
Ethanol
溶媒
HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

1,4-Dihydro-2,6-dimethyl-4-(3-isothiocyanatophenyl)-3,5-pyrazinedicarboxylic acid, dimethyl ester (144 mg, 0.40 mmol) was added into sodium cyanamide (28 mg, 0.44 mmol) in 3 mL of EtOH and the mixture was stirred for 20 minutes. EtOH was then removed in vacuo and the resultant foam-like material was mixed with 4-phenyl-piperidine-1-propanamine (105 mg, 0.48 mmol) in 5 mL of THF. The mixture was cooled down to 0° C. and HgCl2 (109 mg) was added. The reaction was completed in 15 min. After filtration and extraction, the organic layer was concentrated and purified by chromatography (silica gel, eluted with 10% (v/v) methanol in methylene chloride) to yield the title compound as isolated as a yellow foam (175 mg, 75%); 1H-NMR (CDCl3) δ 7.05-7.35 (m, 6H), 6.75 (br, 1H), 6.65 (d, 1H, J=7.5 Hz), 6.58 (d, 1H, J=8.3 Hz), 6.53 (br, 1H), 5.98 (br, 1H), 3.72 (s, 6H), 3.38 (m, 2H), 2.97 (m, 2H), 2.30-2.55 (m, 3H), 2.39 (s, 6H), 2.03 (m, 2H), 1.65-1.80 (m, 4H), 1.40-1.60 (m, 2H); 13C-NMR (CDCl3) δ 166.2, 152.6, 149.4, 129.9, 128.5, 126.9, 126.3, 118.3, 116.3, 112.5, 110.4, 108.7, 54.1, 51.8, 42.4, 41.0, 32.7, 29.8, 25.6, and 17.9.

後処理

  1. customEtOH was then removed in vacuo
  2. waitThe reaction was completed in 15 min
  3. filtrationAfter filtration and extraction
  4. concentrationthe organic layer was concentrated
  5. custompurified by chromatography (silica gel, eluted with 10% (v/v) methanol in methylene chloride)

出典と根拠

ORDレコード
ord-cb6c1ecab6774aa2844db12bb35b7db2
出典データセット
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06177429B1

反応ノート

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