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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539506생성일: 2026년 10월 26일

Carbamate → (Quinolin-3-yl)methanol

https://huagongshe.com/reaction/539506

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참여 물질

역할이름HCID투입량
반응물CarbamateHCID 276—
반응물QuinolineHCID 7047—
반응물Sodium borohydrideHCID 4311764—
용매TetrahydrofuranHCID 8028—
생성물(Quinolin-3-yl)methanolHCID 12662983—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871718B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-081ecec58c714981b4aae8a58db36932
출처 메모uspto-grants-2014_10