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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1038829생성일: 2026년 10월 26일

Hydrochloric Acid → HCID 67129957, 화합물

https://huagongshe.com/reaction/1038829

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodoethanolHCID 12225—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물1-Benzylpiperidine-4-carbonitrileHCID 793383—
반응물tert-Butyl(2-iodoethoxy)dimethylsilaneHCID 11129873—
반응물6-Amino-2,2-dimethyl-2H-benzo[B][1,4]oxazin-3(4H)-oneHCID 13665496—
반응물2,4-Dichlorofuro[3,2-D]pyrimidineHCID 45789968—
반응물tert-Butyl (4-(2-(tert-butyldimethylsilyloxy)ethyl)-1-(2-(2,2-dimethyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-ylamino)furo[3,2-d]pyrimidin-4-yl)piperidin-4-yl)methylcarbamateHCID 70141889—
용매1,4-DioxaneHCID 31275—
생성물HCID 67129957HCID 6712995743%

반응 단계

tert-Butyl (4-(2-(tert-butyldimethylsilyloxy)ethyl)-1-(2-(2,2-dimethyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-ylamino)furo[3,2-d]pyrimidin-4-yl)piperidin-4-yl)methylcarbamate (0.40 g, 0.587 mmol, prepared using AH from 2-iodoethanol with TBDMSCl, AF with 1-benzylpiperidine-4-carbonitrile [Ryan] with tert-butyl(2-iodoethoxy)dimethylsilane, AE, O with Boc2O, G, A with 2,4-dichlorofuro[3,2-d]pyrimidine [ArkPharm] and B with 6-amino-2,2-dimethyl-2H-benzo[b][1,4]oxazin-3(4H)-one [Arkpharm]) and an aqueous solution of aqueous HCl (4 M, 7.34 mL, 29.4 mmol) were dissolved in 1,4-dioxane (15 mL) and stirred for about 4 h at rt. The mixture was concentrated under vacuum and the residue was purified by Prep-TLC (EtOAc/pet ether 1:2) to give 6-(4-(4-(aminomethyl)-4-(2-hydroxyethyl)piperidin-1-yl)furo[3,2-d]pyrimidin-2-ylamino)-2,2-dimethyl-2H-benzo[b][1,4]oxazin-3 (4H)-one (0.121 g, 43%): LC/MS (Table 2, Method h) Rt=1.69 min.; MS m/z: 467 (M+H)+. Syk IC50=A

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08551981B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-081ab9a8269a4e048fe16760cbaa8de9
출처 메모uspto-grants-2013_10