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HRID 1490355作成日:2026年10月27日

(4-Nitrophenyl)methyl (2-mercaptoethyl)carbamate → 4-Nitrobenzyl (1R, 5S,6S)-6-[1(R)-t-butyldimethylsilyloxyethyl]-1-methyl-2-[2-(4-nitrobenzyloxycarbonyl)aminoethylthio]-1-carbapen-2-em-3-carboxylate

https://huagongshe.com/reaction/1490355

反応式

関与物質

役割名称HCID仕込み量
反応物(4-Nitrophenyl)methyl (2-mercaptoethyl)carbamateHCID 3017625—
反応物4-nitrobenzyl (1R, 5S,6S)-2-(2-diethylcarbamoylphenylsulfonyl)-1-methyl-6-[1(R)-t-butyldimethylsilyloxyethyl]-1-carbapen-2-em-3-carboxylateHCID 10974512—
生成物4-Nitrobenzyl (1R, 5S,6S)-6-[1(R)-t-butyldimethylsilyloxyethyl]-1-methyl-2-[2-(4-nitrobenzyloxycarbonyl)aminoethylthio]-1-carbapen-2-em-3-carboxylateHCID 1100704987%

反応手順

Following a procedure similar to that described in Example 19(c), but using 4-nitrobenzyl (1R, 5S,6S)-2-(2-diethylcarbamoylphenylsulfonyl)-1-methyl-6-[1(R)-t-butyldimethylsilyloxyethyl]-1-carbapen-2-em-3-carboxylate (prepared as described in Example 42) and 2-(4-nitrobenzyloxycarbonyl)aminoethylmercaptan as starting materials, in relative proportions similar to those used in that Example, the title compound was obtained in a yield of 87%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05681951
出典データセットuspto-grants-1997_10
ORD IDord-a57d16ba4ced4a31a0353085922c024a
出典メモuspto-grants-1997_10