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HRID 1773791作成日:2026年10月25日

1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamate → (6S)-6-methyl-2-phenoxymethyl-4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyrazine

https://huagongshe.com/reaction/1773791

反応式

関与物質

役割名称HCID仕込み量
反応物1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamateHCID 7023103—
反応物ethyl 1-{2-[(tert-butoxycarbonyl)amino]propyl}-3-(phenoxymethyl)-1H-pyrazole-5-carboxylateHCID 67958408—
反応物HCID 67960066HCID 67960066—
反応物HCID 67960219HCID 67960219—
反応物HCID 178469067HCID 178469067—
生成物(6S)-6-methyl-2-phenoxymethyl-4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyrazineHCID 67960172—

反応手順

The compound was prepared from 5-phenoxymethyl-2H-pyrazole-3-carboxylic acid ethyl ester and (1S)-2-hydroxy-1-methyl-ethyl-carbamic acid tert-butyl ester using the methods described in the preceding examples 11 (rac-2-(2-tert-butoxycarbonylamino-propyl)-5-phenoxymethyl-2H-pyrazole-3-carboxylic acid ethyl ester), 12 (rac-6-methyl-2-phenoxymethyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazin-4-one), and 13 (rac-6-methyl-2-phenoxymethyl-4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyrazine).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09255103B2
出典データセットuspto-grants-2016_02
ORD IDord-2c718bbf2b194f9ea389c0e83de9ef65
出典メモuspto-grants-2016_02