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HRID 455407作成日:2026年10月25日

6-Benzothiazolecarboxylic acid, 2-amino- → (2-Amino-benzothiazol-6-yl)-(cis-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl)-methanone

https://huagongshe.com/reaction/455407

反応式

関与物質

役割名称HCID仕込み量
反応物6-Benzothiazolecarboxylic acid, 2-amino-HCID 66740—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物(4aS,10bR)-1,2,3,4,4a,5,6,10b-Octahydrobenzo[f]quinolineHCID 12327022—
生成物(2-Amino-benzothiazol-6-yl)-(cis-2,3,4a,5,6,10b-hexahydro-1H-benzo[f]quinolin-4-yl)-methanoneHCID 8666714424%

反応手順

The title compound is prepared from 2-amino-benzothiazole-6-carboxylic acid and cis-1,2,3,4,4a,5,6,10b-octahydro-benzo[f]quinoline following a procedure analogous to that described in Example 1 [2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexa-fluorophosphate is used]. Yield: 24% of theory; LC (method 4): tR=1.80 min; Mass spectrum (ESI+): m/z=364 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08497281B2
出典データセットuspto-grants-2013_07
ORD IDord-f0290ae204814bc4904d803198e88585
出典メモuspto-grants-2013_07