戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 539506作成日:2026年10月27日

Carbamate → (Quinolin-3-yl)methanol

https://huagongshe.com/reaction/539506

反応式

関与物質

役割名称HCID仕込み量
反応物CarbamateHCID 276—
反応物QuinolineHCID 7047—
反応物Sodium borohydrideHCID 4311764—
溶媒TetrahydrofuranHCID 8028—
生成物(Quinolin-3-yl)methanolHCID 12662983—

反応手順

Synthesis of compounds ERW1041A, B, C, D, E, and 1069 were synthesized using the methods of Choi et al. Chemistry & Biology, Volume 12, Issue 4, Pages 469-475, except the amino-acid amines are protected by a quinoline-containing carbamate. This quinoline-containing carbamate is synthesized by reducing 3-quinolylcarbaldehyde with sodium borohydride in THF followed by an aqueous workup and flash chromatography yielding 3-quinolylcarbinol. para-Nitro-phenylchloroformate is reacted with 3-quinolylcarbinol in methylene chloride and N-methyl morpholine to give a carbonate of 3-quinoline methanol and para-Nitro-phenol. After purification by flash chromatography, this carbonate is reacted with the methyl ester of the amino acid in neat DMF to give the named compounds.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871718B2
出典データセットuspto-grants-2014_10
ORD IDord-081ecec58c714981b4aae8a58db36932
出典メモuspto-grants-2014_10