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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11865생성일: 2026년 10월 24일

Nitrate → HCID 178418760, 화합물

https://huagongshe.com/ko/reaction/11865

반응식

참여 물질

역할이름HCID투입량
반응물NitrateHCID 943—
반응물TriethylamineHCID 8471—
반응물(S)-2-((4-aminomethylbenzoyl)amino)-5-(N-Boc-2-picolylaminomethyl)valeric AcidHCID 21043758—
용매DimethylformamideHCID 6228—
생성물HCID 178418760HCID 178418760—

반응 단계

The compound obtained in Example 41-5 (0.01 g) was dissolved in DMF (0.3 ml). After the addition of dimethylpyrazolecarboxyamidine nitrate (0.01 g), the mixture was adjusted to pH 8 with triethylamine and stirred for 3 days. The reaction solution was concentrated. Chloroform was added to the residue and the mixture was washed with saturated aqueous solution of sodium hydrogencarbonate. The organic layer was concentrated and dried under reduced pressure. The residue was purified by silica gel column chromatography (5 g, chloroform/methanol/water=7/3/0.5) to obtain the title compound (0.01 g) as white foam. The foam was dissolved in methanol (0.3 ml) and 4 mol/l hydrochloric acid/dioxane solution (0.3 ml) was added dropwise. The mixture was stirred for 3 hours at room temperature. The reaction solution was concentrated and dried under reduced pressure to obtain a crude product (0.01 g). The crude product was purified by silica gel column chromatography (0.5 g, chloroform/methanol/water=7/3/0.5) and 1 mol/l hydrochloric acid was added. The mixture was concentrated to obtain hydrochloride of the title compound (0.01 g) as white foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098215B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-1b8da72fa0b543b09dd1bd7a4a052cdb
출처 메모uspto-grants-2006_08