Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1016663생성일: 2026년 10월 26일
Triethylamine → 1-[[[(4-isothiocyanatophenyl)carbonyl]amino]butyl]-N,N-diethyl-D-lysergamide
https://huagongshe.com/reaction/1016663
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Isothiocyanatobenzoyl chloride | HCID 637654 | — |
| 반응물 | 1-(3-aminobutyl)-N,N-diethyl-D-lysergamide | HCID 22894552 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-[[[(4-isothiocyanatophenyl)carbonyl]amino]butyl]-N,N-diethyl-D-lysergamide | HCID 22894554 | 62.2% |
반응 단계
A solution of 370 mg (0.94 mmol) of 5 in 15 mL of dry THF was cooled to 0° C. and treated with a solution of 190 mg (0.96 mmol) of 6 in 5 mL of dry THF, stirred at 0° C. for 30 minutes and then at room temperature overnight. The reaction mixture was treated with 0.14 mL (1.0 mmol) of triethylamine and stirred at room temperature for 2 hours The reaction mixture was concentrated at reduced pressure. The residue was dissolved in methylene chloride, washed with H2O, dried over anhydrous sodium sulfate and concentrated at reduced pressure. The residue was chromatographed on 200 g of silica gel using 3% methanol in methylene chloride as eluent to yield 325 mg (62%) of 7 as a tan amorphous solid [α]D=+47.5° (c=0.91%; CHCl3).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06476199B1 |
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| 출처 데이터셋 | uspto-grants-2002_11 |
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| ORD ID | ord-c7813d691e3849cc95036e9426a1ea7e |
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| 출처 메모 | uspto-grants-2002_11 |
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