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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469324생성일: 2026년 10월 26일

Thionyl Chloride → 6-(3,6-dichloro-pyridazine-4-carbonyl)-4-methyl-3H-benzoxazol-2-one

https://huagongshe.com/reaction/469324

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물3,6-Dichloropyridazine-4-carboxylic acidHCID 433804—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물4-Methyl-3H-benzooxazol-2-oneHCID 12709336—
용매1,2-DichloroethaneHCID 11—
생성물6-(3,6-dichloro-pyridazine-4-carbonyl)-4-methyl-3H-benzoxazol-2-oneHCID 58181184—

반응 조건

온도100 °C

반응 단계

2.00 mL (27.4 mmol) thionyl chloride were added to 1.92 g (9.95 mmol) 3,6-dichloro-pyridazine-4-carboxylic acid in 10 mL 1,2-dichloroethane and the mixture was refluxed for 2 h. The reaction mixture was evaporated to dryness and coevaporated with 1,2-dichloroethane. Then 5.30 g (39.8 mmol) aluminium trichloride and 1.56 g (10.5 mmol) 4-methyl-3H-benzoxazol-2-one were added and the mixture was stirred for 1 h at 100° C. under a nitrogen atmosphere. Then it was stirred for a further 2 h at 120° C., 3 h at 130° C. and then cooled for 48 h at RT. The mixture was decomposed with ice water and extracted with DCM. The organic phases were combined, washed with water, dried on sodium sulphate, filtered and evaporated down i. vac. The residue was triturated with DIPE, suction filtered and dried.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629137B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-cc30edbc4c1543d59c80220e9fc8cade
출처 메모uspto-grants-2014_01