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Water → N-[2-(4-Fluorophenoxy)ethyl]-N'-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)urea

HRID 30538
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인쇄 미리보기

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HRID 30538 반응식
[F:1][C:2]1[CH:11]=[CH:10][C:5]([O:6][CH2:7][CH2:8][NH2:9])=[CH:4][CH:3]=1.C1([O:18][C:19](=O)[NH:20][C:21]2[C:30]3[CH2:29][CH:28]([OH:31])[CH2:27][CH2:26][C:25]=3[CH:24]=[CH:23][CH:22]=2)C=CC=CC=1.O>CS(C)=O>[F:1][C:2]1[CH:11]=[CH:10][C:5]([O:6][CH2:7][CH2:8][NH:9][C:19]([NH:20][C:21]2[C:30]3[CH2:29][CH:28]([OH:31])[CH2:27][CH2:26][C:25]=3[CH:24]=[CH:23][CH:22]=2)=[O:18])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 31358492-(4-Fluorophenoxy)ethanamineHCID 59731048Phenyl (7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)carbamate

생성물 1

HCID 9798211N-[2-(4-Fluorophenoxy)ethyl]-N'-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)urea수율 89.2%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

To 2-(4-Fluorophenoxy)ethylamine (27.4 mg, 0.18 mmol) was added a solution of (7-Hydroxy-5,6,7,8-tetrahydro-naphthalen-1-yl)-carbamic acid phenyl ester (50.0 mg, 0.18 mmol) in 1.5 mL dimethylsulfoxide. The mixture was stirred for 40 minutes, and then poured into water. The resulting solid was filtered and dried under reduced pressure (54.2 mg, 89.2% yield).

후처리

  1. filtrationThe resulting solid was filtered
  2. customdried under reduced pressure (54.2 mg, 89.2% yield)

출처 및 근거

ORD 기록
ord-a01ed4381c1e4a8b800c8cca04785229
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07423175B2

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