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HRID 1851714생성일: 2026년 10월 27일

Iodoacetic Acid → {2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acid

https://huagongshe.com/reaction/1851714

반응식

참여 물질

역할이름HCID투입량
반응물Iodoacetic AcidHCID 5240—
반응물Sodium hydrideHCID 24758—
반응물Tert-butyl [5-(methoxymethyl)-1,3,4-thiadiazol-2-yl]carbamateHCID 84382575—
용매TetrahydrofuranHCID 8028—
생성물{2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acidHCID 6711689290%

반응 조건

온도60 °C

반응 단계

Iodoacetic acid (409.3 g, 2.2 mol, 1.5 eq) is added in one portion to a solution of tert-butyl [5-(methoxymethyl)-1,3,4-thiadiazol-2-yl]carbamate a13 (360 g, 1.47 mol, 1 eq) in tetrahydrofurane (3 l) at room temperature. Sodium hydride (52.8 g, 2.2 mol, 1.5 eq) is then added portionwise, in 30 minutes, at room temperature. The reaction mixture is heated at 60° C. overnight, and the solvent is evaporated under reduced pressure. Water is added to the residue, the solution is acidified to pH=2 with aqueous 6N HCl, then extracted with CH2Cl2. The organic layer is washed with 10% aqueous sodium thiosulfate and evaporated to dryness to afford 455.7 g of {2-[(tert-butoxy-carbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acid a14 which is used directly in the next step without any further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08957218B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-a5c89827bc5643c2a4dbdcb84fa5fb1c
출처 메모uspto-grants-2015_02