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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | alpha-Methylbenzyl isocyanate | HCID 85760 | — |
| 반응물 | cis-(+/-)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo [2,3-b]indol-4-ol | HCID 88402553 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (+/-)-(3aR*,8aS*)-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo-[2,3-b]indol-4-yl (R)-(alpha-methylbenzyl)carbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05726323 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-cb9d1bc99b9b4ab18c65744a87225d92 |
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| 출처 메모 | uspto-grants-1998_03 |
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