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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17103생성일: 2026년 10월 24일

Dimethylformamide → Bms-066

https://huagongshe.com/ko/reaction/17103

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Trifluoroacetic acidHCID 6422—
반응물Methoxyacetic AcidHCID 12251—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물Bms-066HCID 24825710—

반응 조건

온도80 °C

반응 단계

To a mixture of A215.1-trihydrochloride (1.15 g, 2.76 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.794 g, 4.14 mmol), 1-hydroxybenzotriazole (0.559 g, 4.14 mmol), and diisopropylethylamine (2.90 mL, 16.6 mmol) in anhydrous dimethylformamide (50 mL) was added methoxyacetic acid (0.320 mL, 4.14 mmol). The reaction mixture was stirred at 80° C. for 20 min. During the first 5 min, the suspension became homogeneous. The solvent was removed under reduced pressure, and the residue was diluted with dichloromethane, washed with a saturated aqueous solution of sodium bicarbonate, and dried over anhydrous sodium sulfate. Concentration under pressure followed by purification by flash silica gel chromatography using a mixture of methanol in dichloromethane (2%-5%) afforded 0.890 g (85%) of A228 as yellowish-brown solid. The solid was triturated with methanol to give 0.660 g of A228 as a yellow solid. The filtrate was re-purified on silica gel to give an additional 0.191 g of A228. The compound had an HPLC retention time=1.81 min. (Column: Chromolith SpeedROD 4.6×50 mm—4 min.; Solvent A=10% MeOH, 90% H2O, and 0.1% TFA; Solvent B=90% MeOH, 10% H2O, and 0.1% TFA) and a LC/MS M+1=380.33.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737279B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-63b762c955fe4f098af02c47678316af
출처 메모uspto-grants-2010_06