2,2-Diethoxyacetaldehyde → 8-Bromoisoquinolin-1-ol

HRID 1437312ノート

反応式

HRID 1437312 の反応式
C(OC([O:7][CH2:8][CH3:9])C=O)C.[Br:10][C:11]1[CH:12]=[CH:13][CH:14]=[C:15]2C=1C=[N:18][CH:17]=[CH:16]2>>[Br:10][C:11]1[CH:12]=[CH:13][CH:14]=[C:15]2[C:9]=1[C:8](=[O:7])[NH:18][CH:17]=[CH:16]2

参加物

3

反応物 2

HCID 2196092,2-DiethoxyacetaldehydeHCID 98591348-Bromoisoquinoline

生成物 1

HCID 529877478-Bromoisoquinolin-1-ol

実験手順

The isoquinolin-8-yl system can be prepared from the appropriately substituted benzylamine by cyclocondensation with diethoxy-acetaldehyde (see, for example, K. Kido and Y. Watanabe, Chemical & Pharmaceutical Bulletin, 35(12), 4964-6; 1987). Alternatively 8-bromo-isoquinoline (prepared by the method of F. T. Tyson, J.A.C.S., 1939, 61, N. Briet et al., Tetrahedron (2002), 58(29), 5761-5766 or W. D. Brown, et al., Synthesis (2002), (1), 83-86. 183 can be subjected to N-oxidation and rearrangement to give 8-bromo-2H-isoquinolin-1-one. This can be N-methylated to give 8-bromo-2-methyl-2H-isoquinolin-1-one, an appropriate intermediate for the 2-methyl-1-oxo-1,2-dihydroisoquinolin-8-yl system.

後処理

  1. customBrown, et al., Synthesis (2002), (1), 83-86

出典と根拠

ORDレコード
ord-2159c99b98a247fbbc41fa535c312f58
出典データセット
uspto-grants-2009_11
特許番号
US07622481B2

反応ノート

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