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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393437생성일: 2026년 10월 24일

Diisopropylethylamine → 4-(2,3-dihydro-1,3-dioxo-1H-pyrrolo[3,4-c]pyridin-2-yl)-N-[[1-[(4-methoxyphenyl)methyl]cyclopentyl]carbonyl]-L-phenylalanine

https://huagongshe.com/ko/reaction/393437

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1H,3H-furo(3,4-c)pyridine-1,3-dioneHCID 278398—
반응물Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
반응물4-amino-N-[[1-[(4-methoxyphenyl)methyl]cyclopentyl]carbonyl]-L-phenylalanineHCID 54085750—
용매DichloromethaneHCID 6344—
생성물4-(2,3-dihydro-1,3-dioxo-1H-pyrrolo[3,4-c]pyridin-2-yl)-N-[[1-[(4-methoxyphenyl)methyl]cyclopentyl]carbonyl]-L-phenylalanineHCID 5412915923.1%

반응 단계

A solution of 4-amino-N-[[1-[(4-methoxyphenyl)methyl]cyclopentyl]carbonyl]-L-phenylalanine (98 mg, 0.23 mmol), DIPEA (30 μL, 0.23 mmol) and 3,4-pyridinedicarboxylic acid anhydride (114 mg, 0.77 mmol) in dichloromethane (10 mL) was stirred 18 hr at room temperature. The mixture was concentrated to remove most of the dichloromethane and the residue was taken up in DMF (3 mL). Carbonyl diimidazole (103 mg, 0.64 mmol) was added to the resulting solution and the reaction was allowed to proceed for 18 hr. The resulting mixture was purified directly by RP-HPLC on a 4×30 cm Rainin C-18 column using a gradient of 5 to 95% acetonitrile:water containing 0.75% trifluoroacetic acid at a flow of 49 mL/min over 35 min. The peak eluting at 45.6% acetonitrile was concentrated and lyophilized to give 4-(2,3-dihydro-1,3-dioxo-1H-pyrrolo[3,4-c]pyridin-2-yl)-N-[[1-[(4-methoxyphenyl)methyl]cyclopentyl]carbonyl]-L-phenylalanine (28 mg) HR FABMS: obs. mass 528.2146. Calcd. mass 528.2134 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06806365B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-70e492292fa24a72b88fb47d81828c98
출처 메모uspto-grants-2004_10