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

2,6-Anhydro-5-[(tert-butoxycarbonyl)amino]-3,4,5-trideoxy-L-erythro-hexonic acid → HCID 86672605, 화합물

HRID 470695
노트
인쇄 미리보기

반응식

HRID 470695 반응식
[ClH:1].O1CCOC[CH2:3]1.C(OC([NH:15][C@H:16]1[CH2:24][O:23][C@H:19]([C:20]([OH:22])=[O:21])[CH2:18][CH2:17]1)=O)(C)(C)C>CO>[ClH:1].[NH2:15][C@H:16]1[CH2:24][O:23][C@H:19]([C:20]([O:22][CH3:3])=[O:21])[CH2:18][CH2:17]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 109228122,6-Anhydro-5-[(tert-butoxycarbonyl)amino]-3,4,5-trideoxy-L-erythro-hexonic acidHCID 204431481,4-Dioxane hydrochloride

생성물 1

HCID 86672605HCID 86672605, 화합물수율 100%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

4N hydrochloric acid/1,4-dioxane solution (20 ml) was added to a methanol (5 ml) solution of 2,6-anhydro-5-[(tert-butoxycarbonyl)amino]-3,4,5-trideoxy-L-erythro-hexonic acid (Eur. J. Org. Chem., 2003, 2418-2427) (1.00 g, 4.08 mmol) at room temperature and the resulting mixture was stirred for 20 hours. The reaction mixture was concentrated under reduced pressure to give 0.80 g (100%) of the title compound.

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-5fcc9d1e4e9c42ce8a79ad673fc73def
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08629133B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트