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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42833생성일: 2026년 10월 24일

1,2-Dichloroethane → HCID 67365779, 화합물

https://huagongshe.com/ko/reaction/42833

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물NitrogenHCID 947—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물5-Phenyl-1,3-oxazole-4-carboxylic acidHCID 2776299—
반응물2-{2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-oxazol-5-ylmethyl}-2H-[1,2,3]triazol-4-ylamineHCID 67366051—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물HCID 67365779HCID 67365779—

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 5-phenyl-oxazole-4-carboxylic acid (47 mg, 0.25 mmol) in CH2Cl2 (1.5 mL) was treated at rt with HOBt (40 mg, 0.30 mmol), EDC (119 mg, 0.62 mmol), DMAP (8 mg, 0.06 mmol) and the resulting mixture was stirred at rt for 30 min. 2-{2-[1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-oxazol-5-ylmethyl}-2H-[1,2,3]triazol-4-ylamine (80 mg, 0.25 mmol) in CH2Cl2 (1.0 mL) was then added and the resulting mixture was stirred at rt for 72 h. CH2Cl2 (20 mL) followed by water (15 mL) were added and the aqueous phase was extracted with CH2Cl2. The combined organic phases were washed with water, brine, dried over MgSO4, filtered, and the solvent removed under reduced pressure to give the title compound as a yellow oil. LC-MS-conditions 02: tR=1.17 min, [M+H]+=495.54.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536209B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d09c9e4e9e4d497480759f445fc478c3
출처 메모uspto-grants-2013_09