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

Hydrochloric Acid → 4-(3-Benzyl-ureido)-5-methyl-thiophene-2-carboxylic acid

HRID 583768
노트
인쇄 미리보기

반응식

HRID 583768 반응식
[OH-].[K+].C[O:4][C:5]([C:7]1[S:8][C:9]([CH3:23])=[C:10]([NH:12][C:13]([NH:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:14])[CH:11]=1)=[O:6].Cl>CO.O>[CH3:23][C:9]1[S:8][C:7]([C:5]([OH:6])=[O:4])=[CH:11][C:10]=1[NH:12][C:13]([NH:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 101931415-Methyl-4-(3-benzyl-ureido)-thiophene-2-carboxylic acid methyl ester

생성물 1

HCID 223425214-(3-Benzyl-ureido)-5-methyl-thiophene-2-carboxylic acid

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water
용매

실험 절차

A 2N aqueous potassium hydroxide solution (16 mL) was added to a stirred solution of 5-methyl-4-(3-benzyl-ureido)-thiophene-2-carboxylic acid methyl ester from Step 2 of Example 16 below (0.4 g, 1.3 mmol) in warm methanol (4 mL), and the mixture was heated under reflux. After 1 hour the mixture was cooled, diluted with water (100 mL), and acidified with aqueous HCl. The precipitate was filtered off, rinsed with water, then ethanol, then ether, and dried to afford 0.29 g of 5-methyl-4-(3-benzyl-ureido)-thiophene-2-carboxylic acid; mp 259-260° C.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux
  3. temperatureAfter 1 hour the mixture was cooled
  4. filtrationThe precipitate was filtered off
  5. washrinsed with water
  6. dry with materialethanol, then ether, and dried

출처 및 근거

ORD 기록
ord-1bd0e146d099435aba18930236eb8688
출처 데이터셋
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06924276B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트