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HRID 1177734作成日:2026年10月26日

Methyl 2-(bis((tert-butoxy)carbonyl)amino)prop-2-enoate → 2-(Di-tert-butoxycarbonylamino)-3-(7,7-dimethyl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl)-propionic acid methyl ester

https://huagongshe.com/reaction/1177734

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2-(bis((tert-butoxy)carbonyl)amino)prop-2-enoateHCID 10870342—
反応物7,7-dimethyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridineHCID 21102209—
溶媒MethanolHCID 887—
生成物2-(Di-tert-butoxycarbonylamino)-3-(7,7-dimethyl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl)-propionic acid methyl esterHCID 58864404—

反応手順

To a solution of 7,7-dimethyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine (160 mg) in methanol (3 mL) was added 2-(di-tert-butoxycarbonylamino)-acrylic acid methyl ester (331 mg). A gentle stream of nitrogen was applied and the reaction stirred overnight. In the morning, the volume was greatly reduced. The last traces of solvent were removed under high vacuum to give 490 mg (quant.) which was used without purification. 1H-NMR (CDCl3, 500 MHz) δ 1.24 (s, 3H), 1.26 (s, 3H), 1.38 (s, 18H), 2.33 (d, J=11.3, 1H), 2.57 (d, J=11.3, 1H), 3.09 (dd, J=13.1, 5.5, 1H), 3.15 (dd, J=13.4, 9.5, 1H), 3.35 (d, J=12.8, 1H), 3.57 (d, J=12.8, 1H), 3.68 (s, 3H), 5.13 (dd, J=9.5, 3.7, 1H), 7.16 (s, 1H). Mass spec.: 453.30 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07842808B2
出典データセットuspto-grants-2010_11
ORD IDord-b21808d5f66549d998f50eaa8bc8feca
出典メモuspto-grants-2010_11