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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 982722생성일: 2026년 10월 26일

Diisopropylethylamine → HCID 10391154, 화합물

https://huagongshe.com/reaction/982722

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물(R)-2-(methylamino)-1-pyridin-2-ylethanolHCID 10149007—
반응물N-(4-chlorobenzyl)-2-(chloromethyl)-4-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamideHCID 22563229—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 10391154HCID 1039115465.7%

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온도60 °C

반응 단계

A mixture of N-(4-chlorobenzyl)-2-(chloromethyl)-4-methyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide (113 mg, 0.30 mmol), (1R)-2-(methylamino)-1-pyridin-2-ylethanol (Preparation 28) (100 mg, 0.44 mmol) and diisopropylethylamine (230 μL, 1.32 mmol) in dry DMF (8 mL) was heated to 60° C., becoming a solution. The reaction was stirred for 7 hours at that temperature. After cooling to room temperature, the solution was diluted with water (12 mL). The resulting milky suspension was stirred vigorously for 30 minutes, and then left standing overnight in the refrigerator. The mixture was filtered, and the collected solid was washed with water and dried in vacuo, leaving a white solid. Recrystallization from acetonitrile/water (dissolved with warming 5 mL of acetonitrile, then cooled to 0° C. and then diluted with 1 mL of water, left overnight) gave the title compound (98 mg) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06861438B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-34a0ac25195f4337a17fd9b389e71dde
출처 메모uspto-grants-2005_03