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

Phenylethanolamine → HCID 53636592, 화합물

HRID 1576851
노트
인쇄 미리보기

반응식

HRID 1576851 반응식
[NH:1]([C:5]1[NH:6][CH2:7][CH2:8][CH2:9][N:10]=1)[N+]([O-])=O.N[CH2:12][CH:13]([OH:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C1(C)C(C)=CC=CC=1>O>[NH:6]1[CH2:7][CH2:8][CH2:9][N:10]=[C:5]1[NH:1][CH2:12][CH:13]([OH:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1000PhenylethanolamineHCID 7237O-XyleneHCID 412214N-(1,4,5,6-tetrahydropyrimidin-2-yl)nitramide

생성물 1

HCID 53636592HCID 53636592, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 7.2 parts of 1,4,5,6-tetrahydro-2-nitraminopyrimidine, 7.55 parts of α-(aminomethyl)benzyl alcohol and 12 parts of xylene is stirred and refluxed for 4 hours on a water-tap. The xylene is evaporated and the residue is dissolved in 20 parts of acetone. The product is crystallized at room temperature. It is filtered off and dried, yielding α-(1,4,5,6-tetrahydro-2-pyrimidinylaminomethyl)benzyl alcohol.

후처리

  1. customThe xylene is evaporated
  2. dissolutionthe residue is dissolved in 20 parts of acetone
  3. customThe product is crystallized at room temperature
  4. filtrationIt is filtered off
  5. customdried

출처 및 근거

ORD 기록
ord-0bec084fc055422e9d40942fe724e9ea
출처 데이터셋
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03983133

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트