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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1109845생성일: 2026년 10월 26일

Sodium hydride → 18-(tert-Butoxycarbonyl)-6,12,18-tris(benzyloxy)-7,13-dioxo-6,12,18-triazaoctadecanenitrile

https://huagongshe.com/reaction/1109845

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Tert-butyl N-(benzyloxy)carbamateHCID 736159—
반응물12-(tert-Butoxycarbonyl)-6,12-bis(benzyloxy)-7-oxo-6,12-diazadodecanenitrileHCID 10324034—
반응물Ethyl acetate hexaneHCID 21226206—
용매DimethylformamideHCID 6228—
생성물18-(tert-Butoxycarbonyl)-6,12,18-tris(benzyloxy)-7,13-dioxo-6,12,18-triazaoctadecanenitrileHCID 1048499174%

반응 단계

N-(tert-Butoxycarbonyl )-O-benzylhydroxylamine (1.43 g, 6.40 mmol) was alkylated with (6) (3.00 g, 5.68 mmol) using NaH (80%, 0.19 g, 6.33 mmol) in DMF (100 mL), following the procedure used for (4). Column chromatography on silica gel with 4:1 hexane/EtOAc yielded 3.0 g (74%) of (7) as an oil: NMR δ 1.50 (s, 9 H), 1.40-1.85 (m, 12 H), 2.20-2.50 (m, 6 H), 3.27-3.70 (m, 6 H), 4.75 (s, 6 H), 7.33 (s, 15 H). Anal. (C41H54N4O7) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05322961
출처 데이터셋uspto-grants-1994_06
ORD IDord-00af994a3d514c75a88b6af4ed389672
출처 메모uspto-grants-1994_06