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2-Chlorooxane → N-(2-tetrahydropyranyloxy)-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amine

HRID 1059040
노트
인쇄 미리보기

반응식

HRID 1059040 반응식
[CH2:1]([O:4][N:5]([C:16]([CH3:19])([CH3:18])[CH3:17])[C:6]([CH3:15])([CH3:14])[C:7]([NH:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH:2]=[CH2:3].C(N([C:26](C)(C)[C:27](NC(C)(C)C)=[O:28])O)(C)(C)C.ClC1CCCCO1>>[O:28]1[CH2:27][CH2:26][CH2:3][CH2:2][CH:1]1[O:4][N:5]([C:16]([CH3:19])([CH3:18])[CH3:17])[C:6]([CH3:15])([CH3:14])[C:7]([NH:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 5244002-ChlorooxaneHCID 11207972N-allyloxy-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amineHCID 22182216Tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-hydroxylamine

생성물 1

HCID 22598546N-(2-tetrahydropyranyloxy)-tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-amine수율 33%

실험 절차

The compound is prepared in analogy to compound (204) from tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-hydroxylamine and 2-chlor-tetrahydropyrane in 33% yield as colorless oil.

출처 및 근거

ORD 기록
ord-5f1bdc211ec540fda274bab5a12d973a
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06518326B1

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