Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37051생성일: 2026년 10월 26일
Sodium Iodide → 10-(2-Hydroxypropyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid
https://huagongshe.com/reaction/37051
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-Chloro-2-propanol | HCID 31370 | — |
| 반응물 | Tri-tert-butyl 1,4,7,10-Tetraazacyclododecane-1,4,7-triacetate | HCID 11237632 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 10-(2-Hydroxypropyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid | HCID 60715 | — |
반응 단계
1,4,7,10-Tetraazacyclododecane-4,7,10-triacetic acid tri-t-butyl ester (129 mg, 0.25 mmol) (Example 22(a) ) was dissolved in dimethylformamide. Sodium iodide (7.5 mg, 0.5 mmol), triethylamine (76 mg, 0.75 mmol) and 3-chloro-2-propanol (48 mg, 0.5 mmol) were added to the stirred mixture at ambient temperature. The mixture was stirred for 4 hours at ambient temperature, the temperature was then raised to 100° C. and kept there for 2 hours. The solvent was evaporated, and the residue was dissolved in dichloromethane (2 ml) and washed with water (1 ml). Trifluoroacetic acid (2 ml) was added to the organic phase and the mixture was stirred at ambient temperature for 1 hour. The solvents were evaporated and the residue dissolved in water (4 ml). The aqueous solution was washed with ether (5×2 ml). The aqueous solution was acidified, the water was evaporated, and the title compound was isolated as a hygroscopic white powder. Yield 75 mg (74%) The structure was confirmed by 1HNMR and 13CNMR.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05419893 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-9cb41687c6a448f2af24a576b842a460 |
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| 출처 메모 | uspto-grants-1995_05 |
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