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

Thiourea → HCID 178432392, 화합물

HRID 1032588
노트
인쇄 미리보기

반응식

HRID 1032588 반응식
C([O:4][CH2:5][C:6]1[CH:11]=[C:10](Cl)[N:9]2[N:13]=[C:14]([CH3:16])[N:15]=[C:8]2[N:7]=1)(=O)C.NC(N)=[S:19]>C(O)C>[OH:4][CH2:5][C:6]1[CH:11]=[C:10]([SH:19])[N:9]2[N:13]=[C:14]([CH3:16])[N:15]=[C:8]2[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723790ThioureaHCID 156727765-Acetoxymethyl7-chloro-2-methyl-s-triazolo[1,5-a]pyrimidine

생성물 1

HCID 178432392HCID 178432392, 화합물수율 64.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

In 600 ml of ethanol was dissolved 31 g of 5-acetoxymethyl7-chloro-2-methyl-s-triazolo[1,5-a]pyrimidine, and 29.5 g of thiourea was added thereto and the mixture was refluxed for 10 minutes. The reaction mixture was ice-cooled and resulting precipitated crystal was collected by filtration. The crystal was dissolved in 600 ml of a 5 % potassium hydroxide and the mixture was stirred for 30 minutes, ice-cooled and adjusted to pH 2 with 2N hydrochloric acid. Precipitated crystal was collected by filtration, washed with water and dried to obtain 16.33 g of the title compound.

후처리

  1. additionwas added
  2. temperaturethe mixture was refluxed for 10 minutes
  3. temperaturecooled
  4. customresulting
  5. customprecipitated crystal
  6. filtrationwas collected by filtration
  7. dissolutionThe crystal was dissolved in 600 ml of a 5 % potassium hydroxide
  8. temperatureice-cooled
  9. customPrecipitated crystal
  10. filtrationwas collected by filtration
  11. washwashed with water
  12. customdried

출처 및 근거

ORD 기록
ord-1fec2fd65e8c43b4b11c14bcfaa310d6
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04958019

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트