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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 68551182, 화합물 → HCID 68556127, 화합물

HRID 1854686
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HRID 1854686 반응식
C(OC([N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14](/[CH:17]=[CH:18]/[C:19](=[O:32])[CH2:20][C:21](=[O:31])/[CH:22]=[CH:23]/[C:24]3[CH:29]=[CH:28][C:27]([OH:30])=[CH:26][CH:25]=3)[CH:15]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.C(OC(NC1C=CC(/C=C/C(=O)CC(=O)/C=C/C2C=CC(O)=CC=2)=CC=1)=O)(C)(C)C>C(Cl)(Cl)Cl.CO>[OH:30][C:27]1[CH:28]=[CH:29][C:24](/[CH:23]=[CH:22]/[C:21](=[O:31])[CH2:20][C:19](=[O:32])/[CH:18]=[CH:17]/[C:14]2[CH:15]=[C:16]3[C:11]([CH2:10][CH2:9][NH:8]3)=[CH:12][CH:13]=2)=[CH:25][CH:26]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 68551182HCID 68551182, 화합물HCID 68551589HCID 68551589, 화합물

생성물 1

HCID 68556127HCID 68556127, 화합물

시약·촉매·용매 1

HCID 21584188Chloroform methanol용매

실험 절차

The title compound was synthesized using the same procedure employed for Example 281, but with (1E,6E)-1-[1-(tert-butoxycarbony)-indolin-6-yl]-7-(4-hydroxyphenyl)hepta-1,6-diene-3,5-dione (14 mg, 32 μmol, synthesized in Example 292) as the starting material instead of (1E,6E)-1-[4-(tert-butoxycarbonylamino)phenyl]-7-(4-hydroxyphenyl)hepta-1,6-diene-3,5-dione, and was purified by silica gel chromatography (chloroform/methanol=100/0 to 95/5). The product was obtained as a solid (1.4 mg, 13%) having the following characteristic.

출처 및 근거

ORD 기록
ord-bbe8407fcbbb4cbb8f8f0915c46b1e9c
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962674B2

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