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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480269생성일: 2026년 10월 26일

N,N,N',N'-Tetramethylazodicarboxamide → 2-(2-(4-(4-(3-(tert-butoxycarbonylamino)benzyloxy)phenoxy)-phenyl)acetylamino)benzoic Acid Methyl Ester

https://huagongshe.com/reaction/480269

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylazodicarboxamideHCID 4278—
반응물TributylphosphineHCID 13831—
반응물tert-Butyl (3-(hydroxymethyl)phenyl)carbamateHCID 14523557—
반응물Methyl 2-(4-(4-hydroxyphenoxy)phenylacetamido)benzoateHCID 20602792—
용매Tetrahydrofurane dichloromethaneHCID 21919333—
생성물2-(2-(4-(4-(3-(tert-butoxycarbonylamino)benzyloxy)phenoxy)-phenyl)acetylamino)benzoic Acid Methyl EsterHCID 2060279183%

반응 단계

2-(2-(4-(4-Hydroxyphenoxy)phenyl)acetylamino)benzoic acid methyl ester obtained by the Reference Example 24 (315 mg, 0.83 mmol) was dissolved in 20 ml of methylene chloride-THF mixture (1:1 v/v), added with 3-(tert-butoxycarbonylamino)benzyl alcohol (465 mg, 2.1 mmol), 1,1′-azobis(N,N′-dimethylformamide) (359 mg, 2.08 mmol) and tri-n-butyl phosphine (520 ml, 2.1 mmol) and the reaction mixture was stirred over a night. After completing the reaction, the solvent was removed under reduced pressure and the obtained crude residue was purified by silica gel chromatography (elution solvent; hexane:ethyl acetate 75:25 v/v) to obtain the subject compound (404 mg, 0.693 mmol) in the form of a colorless gummy substance. The result of 1H-NMR was consistent with the above structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06649656B1
출처 데이터셋uspto-grants-2003_11
ORD IDord-c8aa473702e94ae9a3d2f401d66fb394
출처 메모uspto-grants-2003_11