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

Acetic Acid → 3-isopropyl-1H-pyrazol-5(4H)-one

HRID 1987605
노트
인쇄 미리보기

반응식

HRID 1987605 반응식
[C:1]([CH2:6][C:7]([O:9]C)=O)(=O)[CH:2]([CH3:4])[CH3:3].C(O)(=O)C.[NH2:15][NH2:16]>C(O)C>[CH:2]([C:1]1[CH2:6][C:7](=[O:9])[NH:16][N:15]=1)([CH3:4])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 9321HydrazineHCID 2759969Methyl 4-methyl-3-oxopentanoate

생성물 1

HCID 184394413-isopropyl-1H-pyrazol-5(4H)-one

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Methyl isobutyrylacetate (0.5 g, 3.47 mmol) was stirred in ethanol and acetic acid (10:1, 2:0.2 mL) and treated with hydrazine (0.13 mL, 4.16 mmol). After 24 hrs, the resulting solid was filtered off and washed with a minimum amount of ethanol to yield 3-isopropyl-1H-pyrazol-5(4H)-one. Then, the 3-isopropyl-1H-pyrazol-5(4H)-one (0.169 g, 1.34 mmol) and 4-chloroquinoline N-oxide (0.24 g, 1.34 mmol) were stirred in acetic anhydride (1.5 mL) at ambient temperature for 20-30 minutes. The reaction mixture was concentrated and the resulting solid was filtered off and washed with a minimum amount of ether to yield Example 18. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.30 (d, J=6.82 Hz, 6H) 3.98 (bs, 1H) 7.61 (t, J=7.58 Hz, 1H) 7.76-7.82 (m, 1H) 7.93 (d, J=8.34 Hz, 1H) 8.08-8.18 (m, 2H); ESI-MS: m/z calc'd for C15H14ClN3O 287.74. found 288.2 (M+H)+.

후처리

  1. filtrationthe resulting solid was filtered off
  2. washwashed with a minimum amount of ethanol

출처 및 근거

ORD 기록
ord-b0d3109adb5142dc8fa7673aed32f80e
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07550598B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트