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

Sodium Hydroxide → 3-[4-(N-BOC-Piperidin-4-yl)butyloxy]isoxazole-5-carboxylic acid

HRID 1957582
노트
인쇄 미리보기

반응식

HRID 1957582 반응식
[C:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][CH2:16][CH2:17][O:18][C:19]2[CH:23]=[C:22]([C:24]([O:26]C)=[O:25])[O:21][N:20]=2)[CH2:10][CH2:9]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[OH-].[Na+]>CO>[C:1]([N:8]1[CH2:9][CH2:10][CH:11]([CH2:14][CH2:15][CH2:16][CH2:17][O:18][C:19]2[CH:23]=[C:22]([C:24]([OH:26])=[O:25])[O:21][N:20]=2)[CH2:12][CH2:13]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 19068162Methyl 3-[4-(N-BOC-Piperidin-4-yl)butyloxy]isoxazole-5-carboxylate

생성물 1

HCID 190681503-[4-(N-BOC-Piperidin-4-yl)butyloxy]isoxazole-5-carboxylic acid수율 98.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 4-4 (2.7 g, 6.9 mmol), CH3OH (50 mL), and 1N NaOH (13.9 mL, 13.9 mmol) was stirred at ambient temperature for 1 h. The CH3OH was evaporated and the resulting aqueous portion acidified with 1M NaHSO4. The solution was extracted with EtOAc (3×) and then the extracts were combined, dried (MgSO4), and concentrated to give 4-5 (2.5 g) as a solid.

후처리

  1. customThe CH3OH was evaporated
  2. extractionThe solution was extracted with EtOAc (3×)
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-88b2790005fc43e0bd7cb5b799f4e7bd
출처 데이터셋
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05786373

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트