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4-Methoxybenzyl alcohol → tert-butyl N-[(4-methoxyphenyl)methyl]-N-[(E)-N-[(2-methylpropan-2-yl)oxycarbonyl]-C-pyrazol-1-ylcarbonimidoyl]carbamate

HRID 1183041
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HRID 1183041 반응식
[C:1]([O:5][C:6](=[O:33])[N:7](/[C:19](=[N:25]/[C:26]([O:28][C:29]([CH3:32])([CH3:31])[CH3:30])=[O:27])/[N:20]1[CH:24]=[CH:23][CH:22]=[N:21]1)[CH2:8]CCC1C=CC(OC)=CC=1)([CH3:4])([CH3:3])[CH3:2].[CH3:34][O:35][C:36]1[CH:43]=[CH:42][C:39](CO)=[CH:38][CH:37]=1>>[C:1]([O:5][C:6](=[O:33])[N:7](/[C:19](=[N:25]\[C:26]([O:28][C:29]([CH3:30])([CH3:31])[CH3:32])=[O:27])/[N:20]1[CH:24]=[CH:23][CH:22]=[N:21]1)[CH2:8][C:39]1[CH:42]=[CH:43][C:36]([O:35][CH3:34])=[CH:37][CH:38]=1)([CH3:4])([CH3:2])[CH3:3]
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3

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HCID 77384-Methoxybenzyl alcoholHCID 87204231tert-butyl N-[3-(4-methoxyphenyl)propyl]-N-[(Z)-N-[(2-methylpropan-2-yl)oxycarbonyl]-C-pyrazol-1-ylcarbonimidoyl]carbamate

생성물 1

HCID 87331727tert-butyl N-[(4-methoxyphenyl)methyl]-N-[(E)-N-[(2-methylpropan-2-yl)oxycarbonyl]-C-pyrazol-1-ylcarbonimidoyl]carbamate

실험 절차

The title compound is prepared by an analogous procedure to Intermediate E by replacing 3-(4-methoxyphenyl)-1-propanol with 4-methoxybenzylalcohol. [M+H]+ 431.

출처 및 근거

ORD 기록
ord-eaabfc901ab64574a275935f75e21024
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08664228B2

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