돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 591971생성일: 2026년 10월 25일

3-(Dimethylamino)benzaldehyde → HCID 178482749, 화합물

https://huagongshe.com/reaction/591971

반응식

참여 물질

역할이름HCID투입량
반응물3-(Dimethylamino)benzaldehydeHCID 34288—
반응물Ammonium AcetateHCID 517165—
반응물HCID 117701640HCID 117701640—
용매EthanolHCID 702—
생성물HCID 178482749HCID 17848274937.3%

반응 단계

(1S,2S,3R,4R)-3-(2,3-Diamino-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide (50.0 mg, 0.193 mmol) and 3-dimethylamino-benzaldehyde (31.6 mg, 0.212 mmol) were combined with ammonium acetate (29.7 mg, 0.386 mmol) and heated in ethanol (2.5 mL) at 70° C. for 18 h. The reaction mixture was concentrated and chromatographed by reverse phase preparative HPLC. The desired fractions were neutralized with bicarb solution and extracted into EtOAc. The organic layer was dried over MgSO4, filtered and concentrated. This residue was triturated in ethyl ether and filtered to yield 28 mg (37%) of the title compound. mp: 200-204° C., 1H NMR (300 MHz, DMSO-d6): 13.02 (s, 1H), 7.90 (d, 1H), 7.66 (s, 1H), 7.50 (s, 1H), 7.47 (d, J=8 Hz, 1H), 7.30 (t, J=8 Hz, 1H), 7.15 (s, 1H), 6.86 (m, 1H), 6.81 (d, J=8 Hz, 1H), 6.40 (d, J=5 Hz, 1H), 6.33 (s, 2H), 2.98 (s, 6H), 2.87 (s, 1H), 2.77 (s, 1H), 2.60 (d, J=8 Hz, 1H), 2.24 (d, J=8 Hz, 1H), 1.42 (d, J=8 Hz, 1H). HPLC: 1.63 min (G method), MS: 389 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09238656B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-e0796d679f8e49f4bcdfa21ce0e51f25
출처 메모uspto-grants-2016_01