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

Ethanolamine → HCID 59406275, 화합물

HRID 58055
노트
인쇄 미리보기

반응식

HRID 58055 반응식
Cl.[Br:2][C:3]1[CH:4]=[CH:5][C:6]([S:9](Cl)(=[O:11])=[O:10])=[N:7][CH:8]=1.[NH2:13][CH2:14][CH2:15][OH:16].CCN(CC)CC>C(#N)C>[Br:2][C:3]1[CH:4]=[CH:5][C:6]([S:9]([NH:13][CH2:14][CH2:15][OH:16])(=[O:11])=[O:10])=[N:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 700EthanolamineHCID 8471TriethylamineHCID 467388875-Bromopyridine-2-sulfonyl chloride, HCl

생성물 1

HCID 59406275HCID 59406275, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

In a 4 mL vial equipped with a magnetic stir bar were combined 5-bromopyridine-2-sulfonyl chloride hydrochloride (50 mg, 0.171 mmol), 2-aminoethanol (0.015 mL, 0.256 mmol), Et3N (0.071 mL, 0.512 mmol), and acetonitrile (1 mL). The resulting yellow solution stirred at room temperature overnight. The reaction mixture was subsequently partitioned between water (10 mL) and ethyl acetate (15 mL). The layers were separated and the aqueous layer was back-extracted with ethyl acetate (15 mL). The combined organic layers were concentrated to give the title compound as a clear liquid, which was used without further purification (55 mg).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customIn a 4 mL vial equipped with a magnetic stir bar
  2. customThe reaction mixture was subsequently partitioned between water (10 mL) and ethyl acetate (15 mL)
  3. customThe layers were separated
  4. extractionthe aqueous layer was back-extracted with ethyl acetate (15 mL)
  5. concentrationThe combined organic layers were concentrated

출처 및 근거

ORD 기록
ord-cf474c12ee78446ea5f7e28f2d3e3706
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434743B2

반응 노트

불러오는 중…