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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 613216생성일: 2026년 10월 27일

Diisopropylcarbodiimide → HCID 54181953, 화합물

https://huagongshe.com/reaction/613216

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물Tris(2-aminoethyl)amineHCID 77731—
반응물N-HydroxysuccinimideHCID 80170—
반응물N9-(t-butoxycarbonyl)-N6,N9-bis(2-methyl-2-triphenylmethylthiopropyl)-6,9-diazanonanoic acidHCID 53724287—
용매DichloromethaneHCID 6344—
생성물HCID 54181953HCID 54181953—

반응 단계

BAT-BM was prepared as follows. BAT acid (N9 -(t-butoxycarbonyl)-N6,N9 -bis(2-methyl-2-triphenylmethylthiopropyl)-6,9-diazanonanoic acid) (10.03 g, 10.89 mmol) and 75 mL of dry methylene chloride (CH2Cl2) were added to a 250 mL round-bottomed flask equipped with magnetic stir bar and argon balloon. To this solution was added diisopropylcarbodiimide (3.40 mL, 21.7 mmol, 199 mole %), followed by N-hydroxysuccinimide (3.12g, 27.1 mmol, 249 mole %). This solution was observed to become cloudy within 1 h, and was further incubated with stirring for a total of 4 h at room temperature. A solution of tris(2-aminoethyl)amine (30 mL, 200 mmol, 1840 mole %) in 30 mL methylene chloride was then added and stirring continued overnight. The reaction mixture was then concentrated under reduced pressure, and the residue partitioned between ethylacetate (150 mL) and 0.5M potassium carbonate (K2CO3 ; 150 mL). The organic layer was separated, washed with brine and concentrated to give the crude product N-[2-N',N'-bis(2-aminoethyl)aminoethyl)]-N9 -(t-butoxycarbonyl)-N6,N9 -bis(2-methyl-2-triphenylmethylthiopropyl)-6,9-diazanonanamide as a foam/oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06007792
출처 데이터셋uspto-grants-1999_12
ORD IDord-4ab80fdf31b048899b5e73bf88efd563
출처 메모uspto-grants-1999_12