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

Hydrochloric Acid → HCID 131727849, 화합물

HRID 1992352
노트
인쇄 미리보기

반응식

HRID 1992352 반응식
[ClH:1].C(OC([N:9]1[CH2:16][CH:15]2[O:17][CH:11]([CH2:12][N:13]([CH2:18][CH2:19][NH:20][S:21]([C:24]3[CH:29]=[CH:28][C:27]([F:30])=[CH:26][CH:25]=3)(=[O:23])=[O:22])[CH2:14]2)[CH2:10]1)=O)(C)(C)C>O1CCOCC1>[ClH:1].[F:30][C:27]1[CH:28]=[CH:29][C:24]([S:21]([NH:20][CH2:19][CH2:18][N:13]2[CH2:14][CH:15]3[O:17][CH:11]([CH2:10][NH:9][CH2:16]3)[CH2:12]2)(=[O:23])=[O:22])=[CH:25][CH:26]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 68523343HCID 68523343, 화합물

생성물 1

HCID 131727849HCID 131727849, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

HCl in dioxane (50 ml) was added to a solution of 7-[2-(4-Fluoro-benzenesulfonylamino)-ethyl]-9-oxa-3,7-diaza-bicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester (4 g; see step (ii) above) in dry dioxane (50 ml) at RT and the reaction mixture was stirred at RT for 1 h. Dioxane was decanted, precipitated solid was washed with dry diethyl ether (three times) and dried under vacuum to give the title compound as pale yellow solid. Yield: 3.55 g

후처리

  1. customDioxane was decanted
  2. customprecipitated solid
  3. washwas washed with dry diethyl ether (three times)
  4. customdried under vacuum

출처 및 근거

ORD 기록
ord-413f666a4b9340a596d8ee2edb1b990e
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07648985B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트