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2-Methyl-1-nitronaphthalene → Methyl 5-amino-8-bromoisoquinoline-6-carboxylate

HRID 390319
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인쇄 미리보기

반응식

HRID 390319 반응식
[NH2:1][C:2]1[C:11]2[C:6](=[CH:7]C=[CH:9][CH:10]=2)[C:5]([Br:12])=[CH:4][C:3]=1[C:13]([O:15][CH3:16])=[O:14].CC1C=CC2C(=CC=CC=2)C=1[N+:28]([O-])=O.C1(/C=C/B(O)O)C=CC=CC=1.C([B-](F)(F)F)=C.[K+]>>[NH2:1][C:2]1[C:3]([C:13]([O:15][CH3:16])=[O:14])=[CH:4][C:5]([Br:12])=[C:6]2[C:11]=1[CH:10]=[CH:9][N:28]=[CH:7]2
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 134322-Methyl-1-nitronaphthaleneHCID 5702628Styrylboronic acidHCID 23679353Potassium vinyltrifluoroborateHCID 58431835Methyl 1-amino-4-bromonaphthalene-2-carboxylate

생성물 1

HCID 67235893Methyl 5-amino-8-bromoisoquinoline-6-carboxylate

실험 절차

Methyl 5-amino-8-bromoisoquinoline-6-carboxylate was prepared by the procedure described for the synthesis of methyl 1-amino-4-bromo-2-naphthoate in Example 1, substituting 6-methyl-5-nitroisoquinoline for 2-methyl-1-nitronaphthalene and substituting [(E-2-phenylethenyl]boronic acid for potassium vinyltrifluoroborate.

출처 및 근거

ORD 기록
ord-b4e3a413cc954621bc6afd843efa703f
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08383638B2

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