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HRID 133046作成日:2026年10月26日

Ammonia → 4-[4-(6-Methoxy-pyridin-3-ylmethylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-benzoic acid ethyl ester

https://huagongshe.com/reaction/133046

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物2-Methoxy-5-pyridinecarbonitrileHCID 2736776—
反応物(6-Methoxypyridin-3-yl)methanamineHCID 16227379—
反応物4-(4-Chloro-7H-pyrrolo[2,3-D]pyrimidin-6-YL)benzoic acid ethyl esterHCID 23282696—
触媒NickelHCID 935—
溶媒1-ButanolHCID 263—
溶媒MethanolHCID 887—
溶媒TriethylamineHCID 8471—
生成物4-[4-(6-Methoxy-pyridin-3-ylmethylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-benzoic acid ethyl esterHCID 69181635—

反応手順

A mixture of 5.0 g (16.6 mMol) 4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)benzoic acid ethyl ester (WO 97/02266) and 2.52 g (18 mMol) of 6-methoxy-pyridin-3-ylmethylamine (CAS: 262295-96-5; prepared from 6-methoxy-nicotin-nitrile by hydrogenation in the presence of Raney-Nickel in methanol containing NH3) in 3.5 ml (25 mMol) of Et3N and 100 ml n-butanol is heated for 8 h to 140° C. Then additional 0.69 g of 6-methoxy-pyridin-3-ylmethylamine and 1.2 ml of Et3N are added. Heating is continued for 6 h and the hot suspension filtrated and the residue washed with n-butanol and hexane to give the title compound; m.p. 305° C.; elemental analysis for C, H, and N, within 0.5% of calculated value.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390805B2
出典データセットuspto-grants-2008_06
ORD IDord-65edb58ab60148a797105c0667e83bed
出典メモuspto-grants-2008_06