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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1821849생성일: 2026년 10월 24일

Diethyl Ether → HCID 57893455, 화합물

https://huagongshe.com/ko/reaction/1821849

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Ammonium ChlorideHCID 25517—
반응물7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehydeHCID 57893503—
반응물HCID 178418255HCID 178418255—
용매TetrahydrofuranHCID 8028—
생성물HCID 57893455HCID 5789345562%

반응 조건

온도-15 °C

반응 단계

To a solution of 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde (Example 141) (1.7 g, 5.1 mmol) in tetrahydrofuran (25 mL) was added 3.0 M phenylmagnesium bromide in Et2O (2.0 mL, 6 mmol) dropwise at −78° C. under a nitrogen atmosphere. After stirring for ca. 2 h, additional 3.0 M phenylmagnesium bromide in Et2O (2.0 mL, 6 mmol) was added. The reaction mixture was stirred for another 1.5 h warming to −15° C. The reaction mixture was poured into a saturated ammonium chloride solution, and extracted with ethyl acetate (3×). The combined organic extracts were washed with saturated sodium chloride, and dried over sodium sulfate. Filtration and concentration provided the crude material, which was purified by Biotage chromatography (10-30% ethyl acetate in hexanes) to provide [7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl](phenyl)methanol (1.32 g, 62%) as a yellow foam: mp 53-61° C.; 1H NMR (500 MHz, CD3OD) δ4.60 (4H, q, J=23.2, 15.4 Hz), 5.95 (1H, s), 6.25 (1H, s), 7.05 (1H, d, J=5.7 Hz), 7.15-7.40 (15H, m), 7.62 (1H, d, J=5.7 Hz); ESI MS m/z 420 [C28H25N3O+H]+; HPLC (Method A) >99% (AUC), tR=19.2 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07608627B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-e8ef13baa8f14ab4b618b086164db16e
출처 메모uspto-grants-2009_10