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n,n-Bis(2-chloroethyl)-2-methoxyaniline → 1,2,3,4-Tetrahydro-6-hydroxy-2-[4-(2-methoxyphenyl)-1-piperazinyl]-naphthalene

HRID 1660488
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인쇄 미리보기

반응식

HRID 1660488 반응식
Cl[CH2:2][CH2:3][N:4]([CH2:13][CH2:14]Cl)[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[O:11][CH3:12].[NH2:16][CH:17]1[CH2:26][CH2:25][C:24]2[C:19](=[CH:20][CH:21]=[C:22]([OH:27])[CH:23]=2)[CH2:18]1>C(O)C>[OH:27][C:22]1[CH:23]=[C:24]2[C:19](=[CH:20][CH:21]=1)[CH2:18][CH:17]([N:16]1[CH2:14][CH2:13][N:4]([C:5]3[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=3[O:11][CH3:12])[CH2:3][CH2:2]1)[CH2:26][CH2:25]2
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참가 물질

4

반응물 2

HCID 227137n,n-Bis(2-chloroethyl)-2-methoxyanilineHCID 131778796-Amino-5,6,7,8-tetrahydronaphthalen-2-OL

생성물 1

HCID 205568141,2,3,4-Tetrahydro-6-hydroxy-2-[4-(2-methoxyphenyl)-1-piperazinyl]-naphthalene

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2.48 g of N,N-Di(2-chloroethyl)-2-methoxyaniline are dissolved together with 1.63 g of 2-amino-1,2,3,4-tetrahydro-6-hydroxynaphthalene in 100 ml of ethanol and finally refluxed for 20 hours. The solvent is evaporated off and the residue recrystallized from methanol/ether to yield the title compound. M.P. 282°-286° [Hydrochloride salt form].

후처리

  1. temperaturefinally refluxed for 20 hours
  2. customThe solvent is evaporated off
  3. customthe residue recrystallized from methanol/ether

출처 및 근거

ORD 기록
ord-cae9cf9f7e7c4e7684699a47f1e0a275
출처 데이터셋
uspto-grants-1981_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04308266

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