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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220958생성일: 2026년 10월 27일

Ammonium Chloride → (4-Aminomethyl-3-methyl-phenyl)-(3,6-dimethyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulen-9-yl)-methanone

https://huagongshe.com/reaction/220958

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물1,2,3,4-Tetrahydro-benzo(b)azepin-5-oneHCID 294788—
반응물RiboflavinHCID 493570—
반응물Sodium borohydrideHCID 4311764—
반응물4-(3,6-Dimethyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-2-methyl-benzonitrileHCID 135736040—
촉매Dichlorocobalt hexahydrateHCID 517166—
용매MethanolHCID 887—
생성물(4-Aminomethyl-3-methyl-phenyl)-(3,6-dimethyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulen-9-yl)-methanoneHCID 13573605335%

반응 단계

A solution of 4-(3,6-dimethyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-2-methyl-benzonitrile from Example E101.1 (1.42 g, 4.0 mmol) in methanol (50 ml) at 0° C. was treated with cobalt(II) chloride hexahydrate (1.90 g, 8.0 mmol). The mixture was stirred for 15 min at room temperature then sodium borohydride (1.51 g, 40.0 mmol) was added portionwise. The reaction mixture was stirred for 2 h then saturated NH4Cl was added. The mixture was stirred for 30 min then the solid was filtered off through Celite® filter agent and the filtrate concentrated in vacuo. The residue was re-dissolved in EtOAc and saturated NaHCO3. The layers were partitioned and the aqueous layer was extracted further with chloroform. Organics were combined, dried and concentrated in vacuo. The residue was purified by flash chromatography on silica gel through an isolute (eluant; 1% 35% ammonia:9% methanol:90% dichloro-methane) to yield the title compound (511 mg, 35%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202858B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a43f03a49b7c473382257548c67b4054
출처 메모uspto-grants-2012_06