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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1770생성일: 2026년 10월 23일

1,8-Diazabicyclo(5.4.0)undec-7-ene → (+/-)-(3aR*,8aS*)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo-[2,3-b]indol-4-yl (R)-(alpha-methylbenzyl)carbamate

https://huagongshe.com/ko/reaction/1770

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물alpha-Methylbenzyl isocyanateHCID 85760—
반응물cis-(+/-)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo [2,3-b]indol-4-olHCID 88402553—
용매TetrahydrofuranHCID 8028—
생성물(+/-)-(3aR*,8aS*)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo-[2,3-b]indol-4-yl (R)-(alpha-methylbenzyl)carbamateHCID 53984692—

반응 단계

cis-(±)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo [2,3-b]indol-4-ol (2g) was dissolved in degassed THF (200 ml). DBU (0.8 ml) was added to the mixture followed by R-(+)-α-methylbenzyl isocyanate (2 g). The reaction was stirred at room temperature overnight under nitrogen. The solvent was evaporated under reduced pressure and the residue was purified using Prep 500 chromatography (4% MeOH/DCM) to yield 1.2 g of a solid. This material was combined with 600 mg of identically prepared material, which was found to be pure by thin layer analysis. The combined product was triturated with isopropyl ether and filtered to yield 1.8 g of (±)-(3aR*, 8aS*)-1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo [2,3-b]indol-4-yl (R)-(α-methylbenzyl)carbamate, m.p. 151°-155° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726323
출처 데이터셋uspto-grants-1998_03
ORD IDord-cb9d1bc99b9b4ab18c65744a87225d92
출처 메모uspto-grants-1998_03