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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1931713생성일: 2026년 10월 25일

2,2-Dimethylpropyl carbonochloridate → 4-[4-(4-Methanesulfonyl-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid 2,2-dimethyl-propyl ester

https://huagongshe.com/reaction/1931713

반응식

참여 물질

역할이름HCID투입량
반응물2,2-Dimethylpropyl carbonochloridateHCID 3352185—
반응물4-(4-methanesulfonyl-phenoxy)-1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine trifluoroacetate saltHCID 66915326—
생성물4-[4-(4-Methanesulfonyl-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid 2,2-dimethyl-propyl esterHCID 57964945—

반응 단계

4-[4-(4-Methanesulfonyl-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid 2,2-dimethyl-propyl ester was prepared according to General Procedure E by the reaction of 4-(4-methanesulfonyl-phenoxy)-1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine trifluoro-acetate salt (Intermediate 27) with 2,2-dimethylpropyl chloroformate (available from Aldrich Chemical Company, Inc., Milwaukee, Wis., USA). 1H NMR (400 MHz, DMSO-d6) δ 0.93 (s, 9H), 1.98-2.01 (m, 4H), 3.00-3.10 (m, 2H), 3.30 (methyl sulfonyl and water peak), 3.70-3.80 (m, 2H), 4.14-4.17 (m, 2H), 5.03-5.09 (m, 1H), 7.63-7.65 (m, 2H), 8.05-8.07 (m, 2H), 8.37 (s, 1H), 8.57 (s, 1H). Mass spectrum MH+=488.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08188098B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-6f894a935d6b434ca5737df07dc0c3ce
출처 메모uspto-grants-2012_05