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Sodium Bicarbonate → 4,5-Bis(4-methoxyphenyl)-2-(3-isopropylureidomethyl)thiazole

HRID 1885566
ノート
印刷プレビュー

反応式

HRID 1885566 の反応式
Cl.[NH2:2][CH2:3][C:4]1[S:5][C:6]([C:17]2[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[CH:19][CH:18]=2)=[C:7]([C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=2)[N:8]=1.[C:25](=[O:28])([O-])O.[Na+].NCC1S[C:34](C2C=CC(OC)=CC=2)=[C:35]([C:37]2C=CC(OC)=CC=2)[N:36]=1>ClCCl>[CH3:16][O:15][C:12]1[CH:11]=[CH:10][C:9]([C:7]2[N:8]=[C:4]([CH2:3][NH:2][C:25]([NH:36][CH:35]([CH3:37])[CH3:34])=[O:28])[S:5][C:6]=2[C:17]2[CH:18]=[CH:19][C:20]([O:23][CH3:24])=[CH:21][CH:22]=2)=[CH:14][CH:13]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 516892Sodium BicarbonateHCID 99736622-Aminomethyl-4,5-bis(4-methoxyphenyl)thiazoleHCID 197488812-Aminomethyl-4,5-bis(4-methoxyphenyl)thiazole hydrochloride

生成物 1

HCID 104317614,5-Bis(4-methoxyphenyl)-2-(3-isopropylureidomethyl)thiazole

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

2-Aminomethyl-4,5-bis(4-methoxyphenyl)thiazole hydrochloride (1.00 g) was added to a mixture of dichloromethane and saturated aqueous sodium hydrogencarbonate, and 2-aminomethyl-4,5-bis(4-methoxyphenyl)thiazole was extracted with dichloromethane. The separated organic layer was washed with water and brine, and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo and the resulting residue was dissolved with tetrahydrofuran (20 ml) and methanol (7 ml). N-Isopropyl isocyanate (0.38 ml) was added thereto, and the reaction mixture was stirred at ambient temperature for 90 minutes. The reaction mixture was evaporated in vacuo, and the resulting powder was triturated with isopropyl ether, to give 4,5-bis(4-methoxyphenyl)-2-(3-isopropylureidomethyl)thiazole (1.04 g).

後処理

  1. extractionwas extracted with dichloromethane
  2. washThe separated organic layer was washed with water and brine
  3. dry with materialdried over magnesium sulfate
  4. filtrationAfter filtration
  5. customthe filtrate was evaporated in vacuo
  6. dissolutionthe resulting residue was dissolved with tetrahydrofuran (20 ml) and methanol (7 ml)
  7. additionN-Isopropyl isocyanate (0.38 ml) was added
  8. customThe reaction mixture was evaporated in vacuo
  9. customthe resulting powder was triturated with isopropyl ether

出典と根拠

ORDレコード
ord-498b298bcfa244949abc2686d80b1cad
出典データセット
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05145860

反応ノート

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