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

Uracil, 6-amino-3-methyl-1-propyl- → HCID 14425321, 화합물

HRID 1086814
노트
인쇄 미리보기

반응식

HRID 1086814 반응식
[NH2:1][C:2]1[N:7]([CH2:8][CH2:9][CH3:10])[C:6](=[O:11])[N:5]([CH3:12])[C:4](=[O:13])[CH:3]=1.[N:14]([O-])=[O:15].[Na+]>C(O)(=O)C.O>[NH2:1][C:2]1[N:7]([CH2:8][CH2:9][CH3:10])[C:6](=[O:11])[N:5]([CH3:12])[C:4](=[O:13])[C:3]=1[N:14]=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 104563Uracil, 6-amino-3-methyl-1-propyl-HCID 23668193Sodium Nitrite

생성물 1

HCID 14425321HCID 14425321, 화합물수율 83%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

실험 절차

6-Amino-3-methyl-1-n-propyluracil (10.46 g, 57.8 mmol) was dissolved in 10 ml of acetic acid at 90° C. Then, with stirring, a solution of sodium nitrite (4.19 g, 60.8 mmol) in 100 ml of water was added in 10 ml portions over 5 minutes. A purple color formed immediately followed by a purple precipitate. The mixture was cooled in the freezer for 20 minutes and then the precipitate was collected by vacuum filtration, washed with water (2×30 ml) and acetone (2×10 ml), and air-dried to give 6-amino-3-methyl-5-nitroso-1-n-propyluracil as purple needles (10.02 g, 83%). 1H NMR (DMSO-d6 +D2O) δ0.89 (t, J=8 Hz, 3 H), 1.55 (sextet, J=8 Hz, 2 H), 3.27 (s, 3 H), 3.80 (t, J=8 Hz, 2 H).

후처리

  1. customA purple color formed immediately
  2. temperatureThe mixture was cooled in the freezer for 20 minutes
  3. filtrationthe precipitate was collected by vacuum filtration
  4. washwashed with water (2×30 ml) and acetone (2×10 ml)
  5. customair-dried

출처 및 근거

ORD 기록
ord-4ae0e829900845139036fc8ae49340f3
출처 데이터셋
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05032593

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트