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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131656생성일: 2026년 10월 26일

3-Heptanone → 2-(s)-(1-Propyl-butylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide

https://huagongshe.com/reaction/131656

반응식

참여 물질

역할이름HCID투입량
반응물3-HeptanoneHCID 7802—
반응물Sodium SulfateHCID 24436—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물2-(S)-amino-pentanoic acid [5-(5-methoxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide HCl saltHCID 131726918—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매1,1-DichloroethaneHCID 6365—
생성물2-(s)-(1-Propyl-butylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amideHCID 11654783—

반응 조건

온도40 °C

반응 단계

A mixture of 2-(S)-amino-pentanoic acid [5-(5-methoxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide HCl salt (100 mg, 0.265 mmol) and 3-heptanone (0.1 mL), acetic acid (0.2 mL), sodium sulfate and sodium cyanoborohydride (100 mg) in dichloroethane (2 mL) and methanol (1 mL) was stirred at 40° C. overnight. The mixture was quenched with water, basified by dilute sodium hydroxide, and extracted with methylene chloride. The organic layer was concentrated to dryness. The residue was purified by Biotage silica gel column chromatography to isolate 2-(S)-(1-propyl-butylamino)-pentanoic acid [5-(5-hydroxy-1,5-dimethyl-hexyl)-thiazol-2-yl]-amide as a colorless oil, LC-MS, RT=2.2 min, M+1=426.5.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384968B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-59679df6d87c47658f1cf87b4a0d71bc
출처 메모uspto-grants-2008_06