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

HCID 20267946, 화합물 → 3-[(Chloromethoxy)methyl]-1,2,5-thiadiazole

HRID 1719235
노트
인쇄 미리보기

반응식

HRID 1719235 반응식
S(Cl)(Cl)(=O)=O.[Cl:6][CH2:7][O:8][CH2:9][C:10]1[CH:14]=[N:13][S:12][N:11]=1.CSCOCC1C=NSN=1>ClCCl>[Cl:6][CH2:7][O:8][CH2:9][C:10]1[CH:14]=[N:13][S:12][N:11]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 20267946HCID 20267946, 화합물HCID 86740280HCID 86740280, 화합물

생성물 1

HCID 202679333-[(Chloromethoxy)methyl]-1,2,5-thiadiazole

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

반응 조건

온도
0 °C

실험 절차

3-(Chloromethyloxymethyl)-1,2,5-thiadiazole Sulfuryl chloride (0.24 mmol) in dry dichloromethane (0.5 ml) was added dropwise over a period of 3 minutes at 0° C. to a solution of 3-(Methylthiomethyloxy)methyl-1,2,5-thiadiazole (0.24 mmol) in dry dichloromethane (1.5 ml). The mixture was stirred at 0° C. for 5 minutes and at room temperature for 10 minutes before the solution was evaporated at reduced pressure. The crude product (30 mg, 75%) was used for alkylation in Example 9 without any further purification.

후처리

  1. customwas evaporated at reduced pressure
  2. customThe crude product (30 mg, 75%) was used for alkylation in Example 9 without any further purification

출처 및 근거

ORD 기록
ord-083b88cce4a9445282ab2e9db73c84c2
출처 데이터셋
uspto-grants-1985_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04539324

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트