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HRID 274774作成日:2026年10月25日

N-[(S)-alpha-[(t-butylsulphonyl)methyl]hydrocinnamoyl]-3-(2,4-dinitrophenyl)-L-histidine → HCID 178455618、化合物

https://huagongshe.com/reaction/274774

反応式

関与物質

役割名称HCID仕込み量
反応物N-[(S)-alpha-[(t-butylsulphonyl)methyl]hydrocinnamoyl]-3-(2,4-dinitrophenyl)-L-histidineHCID 22845096—
反応物(1RS,2R,3S)-3-amino-4-cyclohexyl-1-(2-furyl)-1,2-butanediolHCID 57084513—
生成物HCID 178455618HCID 178455618—

反応手順

In an analogous manner to that described in Example 13, by reacting (1RS,2R,3S)-3-amino-4-cyclohexyl-1-(2-furyl)-1,2-butanediol with N-[(S)-α-[(t-butylsulphonyl)methyl]hydrocinnamoyl]-3-(2,4-dinitrophenyl)-L-histidine there was obtained (S)-α-[(S)-α-[(t-butylsulphonyl)methyl]hydrocinnamamido]-N-[(1S,2R,3RS)-1-(cyclohexylmethyl)-2,3-dihydroxy-3-(2-furyl)propyl]imidazole-4-propionamide (1:1 mixture of epimers) as a pale yellow solid, MS: 657 (M+H)+. The more polar epimer (S)-α-[(S)-α-[(t-butylsulphonyl)methyl]hydrocinnamamido]-N-[(1S,2R,3R or S)-1-(cyclohexylmethyl)-2,3-dihydroxy-3-(2-furyl)propyl]imidazole-4-propionamide, MS: 657 (M+H)+, can be separated from the above mixture by chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05389616
出典データセットuspto-grants-1995_02
ORD IDord-cb7dd0edd96046cd9f7e38256fe62846
出典メモuspto-grants-1995_02