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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 707383생성일: 2026년 10월 26일

Diisopropylethylamine → HCID 178429379, 화합물

https://huagongshe.com/reaction/707383

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-(Methylsulfonyl)thiazolo[5,4-b]pyridineHCID 3604503—
반응물HCID 178429369HCID 178429369—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물HCID 178429379HCID 17842937960.5%

반응 조건

온도100 °C

반응 단계

A mixture of 5-(trans-3-aminocyclobutyl)-7,7-dimethyl-5H-pyrrolo[2,3-b]pyrazin-6(7H)-one dihydrochloride (Intermediate 83, 51 mg, 0.167 mmol), N-ethyl-N-isopropylpropan-2-amine (102 μl, 0.585 mmol), and 2-(methylsulfonyl)thiazolo[5,4-b]pyridine (Intermediate 76) (43.0 mg, 0.201 mmol) in DMSO (0.3 ml) was stirred at 100° C. for 3 h. The mixture was diluted with EtOAc and water in a separatory funnel. The aqueous layer was extracted with EtOAc twice. The combined organic layer was dried over Na2SO4 and concentrated in vacuo. The crude solution was purified by silica gel chromatography (ISCO 12 g, 0-70% EtOAc-hexane) to give 7,7-dimethyl-5-(trans-3-(thiazolo[5,4-b]pyridin-2-ylamino)cyclobutyl)-5H-pyrrolo[2,3-b]pyrazin-6(7H)-one (37 mg, 0.101 mmol, 60.4% yield) as off-white solid. 1H NMR (300 MHz, CHLOROFORM-d) δ ppm 1.46 (s, 6 H) 2.50 (ddd, J=14.03, 9.35, 3.51 Hz, 2 H) 3.37-3.55 (m, 2 H) 5.30 (t, J=8.48 Hz, 1 H) 5.73 (br. s., 1 H) 7.17-7.25 (m, 1 H) 7.74 (dd, J=8.04, 1.46 Hz, 1 H) 8.05-8.16 (m, 2 H) 8.22 (dd, J=4.75, 1.53 Hz, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09174992B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-cba2053e67e34362bcc5567ab35ee0e6
출처 메모uspto-grants-2015_11