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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1184654생성일: 2026년 10월 27일

2-Chloroethyl isocyanate → {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl} (2-chloroethyl)carbamate

https://huagongshe.com/reaction/1184654

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참여 물질

역할이름HCID투입량
반응물2-Chloroethyl isocyanateHCID 16035—
반응물TolvaptanHCID 216237—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TolueneHCID 1140—
생성물{7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl} (2-chloroethyl)carbamateHCID 8670893782%

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온도80 °C

반응 단계

Tolvaptan (1.0 g, 2.2 mmol) was suspended in toluene (7 ml). 2-Chloroethyl isocyanate (0.28 ml, 3.3 mmol) and 4-dimethylaminopyridine (DMAP) (27 mg, 0.22 mmol) were added thereto, and the mixture was stirred at 80° C. for 24 hours. After cooling to room temperature, the insoluble materials were filtered off and washed with ethyl acetate. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (n-hexane:ethyl acetate=54:46→33:67). The purified product was concentrated under reduced pressure to obtain 1.0 g of {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}(2-chloroethyl)carbamate as white amorphous solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08669229B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-9557162d57b747b49db1b568ee972bde
출처 메모uspto-grants-2014_03