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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(S)-2-phenyl-3-tert-butyl-5-hydroxymethyloxazolidine → 2-(3-tert. Butylamino-2-acetoxypropoxy)-3-cyanopyridine

HRID 972734
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인쇄 미리보기

반응식

HRID 972734 반응식
C1(C2[N:11](C(C)C)[CH2:10]C(CO)O2)C=CC=CC=1.C[C@H]1N(C(CC)C)CC(CO)[O:19]1.[CH:29]([N:32]1[CH2:36][CH:35]([CH2:37]O)OC1)([CH3:31])C.[C:39]1([C@H:45]2[N:49]([C:50]([CH3:53])([CH3:52])[CH3:51])[CH2:48][CH:47]([CH2:54][OH:55])[O:46]2)C=CC=CC=1>>[C:50]([NH:49][CH2:48][CH:47]([O:46][C:45](=[O:19])[CH3:39])[CH2:54][O:55][C:36]1[C:35]([C:10]#[N:11])=[CH:37][CH:31]=[CH:29][N:32]=1)([CH3:51])([CH3:52])[CH3:53]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 12296652(S)-2-phenyl-3-tert-butyl-5-hydroxymethyloxazolidineHCID 125661982-Phenyl-3-isopropyl-5-hydroxymethyloxazolidineHCID 213212873-Isopropyl-5-hydroxymethyloxazolidineHCID 131710938(S)-2-methyl-3-sec. butyl-5-hydroxymethyloxazolidine

생성물 1

HCID 1317109372-(3-tert. Butylamino-2-acetoxypropoxy)-3-cyanopyridine

실험 절차

Isopropyl or sec. butyl amino analogues of the compounds of the above examples are prepared by substituting suitable oxazolidines e.g. 2-phenyl-3-isopropyl-5-hydroxymethyloxazolidine, (S)-2-methyl-3-sec. butyl-5-hydroxymethyloxazolidine, 3-isopropyl-5-hydroxymethyloxazolidine for the (S)-2-phenyl-3-tert. butyl-5-hydroxymethyloxazolidine reactant.

출처 및 근거

ORD 기록
ord-ea3ecd972f3c4c1cb8daf722628683da
출처 데이터셋
uspto-grants-1977_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04053605

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