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HRID 2294852作成日:2026年10月26日

Oxalate → 6-Acetyl-3-(2-(4-(6-chlorobenzothiazol-2-yl)piperazin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine

https://huagongshe.com/reaction/2294852

反応式

関与物質

役割名称HCID仕込み量
反応物OxalateHCID 71081—
反応物6-Chloro-2-(piperazin-1-yl)-1,3-benzothiazoleHCID 2746595—
反応物6-Acetyl-3-(2-chloroethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridineHCID 21471856—
生成物6-Acetyl-3-(2-(4-(6-chlorobenzothiazol-2-yl)piperazin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridineHCID 2147199910.9%

反応手順

The reaction and procedure were conducted in a similar manner as in Example 24 using 0.2 g of 6-acetyl-3-(2-chloroethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine and 0.2 g of 1-(6-chlorobenzothiazol-2-yl)piperazine to give 0.04 g of 6-acetyl-3-(2-(4-(6-chlorobenzothiazol-2-yl)piperazin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine as an oil, m.p. 180° C. (decomposition) as an oxalate thereof.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05691330
出典データセットuspto-grants-1997_11
ORD IDord-0b5093efc8e545ea90787db95e779a3b
出典メモuspto-grants-1997_11