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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Aminoacetaldehyde dimethyl acetal → N-(2,2-Dimethoxyethyl)-N'-(3-iodophenyl)urea

HRID 857123
노트
인쇄 미리보기

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HRID 857123 반응식
[I:1][C:2]1[CH:3]=[C:4]([N:8]=[C:9]=[O:10])[CH:5]=[CH:6][CH:7]=1.[CH3:11][O:12][CH:13]([O:16][CH3:17])[CH2:14][NH2:15]>C(Cl)Cl>[CH3:11][O:12][CH:13]([O:16][CH3:17])[CH2:14][NH:15][C:9]([NH:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([I:1])[CH:3]=1)=[O:10]
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참가 물질

4

반응물 2

HCID 89728Aminoacetaldehyde dimethyl acetalHCID 44990001-Iodo-3-isocyanatobenzene

생성물 1

HCID 21867194N-(2,2-Dimethoxyethyl)-N'-(3-iodophenyl)urea

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
20 °C

실험 절차

A suspension of 3-iodophenylisocyanate (1.1 g) in DCM (10 ml) was treated with aminoacetaldehyde dimethyl acetal (0.49 ml) and stirred under nitrogen at 20° C. for 24 h. The reaction mixture was quenched by adding MeOH. The solvents were removed under reduced pressure to give the title compound (1.35 g) LCMS RT=2.92 min.

후처리

  1. customThe reaction mixture was quenched
  2. additionby adding MeOH
  3. customThe solvents were removed under reduced pressure

출처 및 근거

ORD 기록
ord-05b5adbcf5534c8fbac6b3df4bc730fc
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07144908B2

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