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

Hydrochloric Acid → HCID 178508042, 화합물

HRID 547383
노트
인쇄 미리보기

반응식

HRID 547383 반응식
[NH2:1][C:2]1[C:7]([NH:8][C:9](=[O:18])[O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:6][CH:5]=[CH:4][N:3]=1.ClC1C=CC=C(C(OO)=[O:27])C=1.Cl>CC(C)=O>[NH2:1][C:2]1[C:7]([NH:8][C:9](=[O:18])[O:10][CH2:11][C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:27]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 70297m-Chloroperbenzoic acidHCID 13451701Benzyl (2-aminopyridin-3-yl)carbamate

생성물 1

HCID 178508042HCID 178508042, 화합물

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

To a solution of benzyl (2-aminopyridin-3-yl)carbamate in acetone was added a solution of m-chloro perbenzoic acid in acetone and the suspension was stirred at room temperature. After 2 hours the suspension was cooled to 0° C., HCl (2N in Et2O) was added, and the precipitate filtered. To the precipitate was added saturated aqueous NaHCO3, EtOAc and MeOH and the mixture stirred until dissolution. The solution was evaporated and the residue washed with water until the pH of the filtrate was neutral. The solid was dried under vacuum.

후처리

  1. temperatureAfter 2 hours the suspension was cooled to 0° C.
  2. filtrationthe precipitate filtered
  3. additionTo the precipitate was added saturated aqueous NaHCO3, EtOAc and MeOH
  4. stirringthe mixture stirred until dissolution
  5. customThe solution was evaporated
  6. washthe residue washed with water until the pH of the filtrate
  7. customThe solid was dried under vacuum

출처 및 근거

ORD 기록
ord-4b8f859f683c49b9ad974d223eaa024d
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07939537B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트