홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

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

HRID 1885566
노트
인쇄 미리보기

반응식

HRID 1885566 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-498b298bcfa244949abc2686d80b1cad
출처 데이터셋
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05145860

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트