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4-Quinolinecarboxaldehyde → HCID 87565005, 화합물

HRID 1169640
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HRID 1169640 반응식
[NH:1]([C:7](OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=[O:8])[CH:2](O)[C:3]([OH:5])=[O:4].[N:24]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[C:27]([CH:34]=O)=[CH:26][CH:25]=1.[F:36][C:37]([F:49])([F:48])[S:38]([C:41]1[CH:47]=[CH:46][C:44]([NH2:45])=[CH:43][CH:42]=1)(=[O:40])=[O:39]>>[F:36][C:37]([F:49])([F:48])[C:3]([OH:5])=[O:4].[N:24]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[C:27]([CH2:34][N:1]2[CH2:2][C:3](=[O:4])[N:45]([C:44]3[CH:46]=[CH:47][C:41]([S:38]([C:37]([F:48])([F:36])[F:49])(=[O:39])=[O:40])=[CH:42][CH:43]=3)[C:7]2=[O:8])=[CH:26][CH:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 780724-QuinolinecarboxaldehydeHCID 1363154-Aminophenyl trifluoromethyl sulphoneHCID 60112698HCID 60112698, 화합물

생성물 1

HCID 87565005HCID 87565005, 화합물수율 35.5%

실험 절차

The compound is prepared from 4 mmol of resin, 12 mmol of N-Fmoc-Gly(OH), 20 mmol of 4-quinolinecarboxaldehyde, and 10 mmol of 4-(trifluoromethanesulfonyl)aniline, in the same way as in Example 1. After purification by preparative LC-MS, 1 g of expected product is obtained.

후처리

  1. customAfter purification by preparative LC-MS

출처 및 근거

ORD 기록
ord-a50d01d5f6eb4451a5c8460985c04c36
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07825115B2

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