Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20849생성일: 2026년 10월 24일
Dicyclohexylcarbodiimide → 4-Chloro-N-[[1-(dimethylamino)cyclopentyl](phenyl)methyl]-2-methylbenzamide
https://huagongshe.com/ko/reaction/20849
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 반응물 | 4-Chloro-2-methylbenzoic acid | HCID 348269 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | {1-[Amino(phenyl)methyl]cyclopentyl}dimethylamine | HCID 11521393 | — |
| 반응물 | (+/-)N-[[3-(Dimethylamino)tetrahydro-3-furanyl](phenyl)methyl]-2,6-dimethylbenzamide | HCID 59347760 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Chloro-N-[[1-(dimethylamino)cyclopentyl](phenyl)methyl]-2-methylbenzamide | HCID 59347782 | 43% |
반응 단계
A mixture of {1-[amino(phenyl)methyl]cyclopentyl}dimethylamine D3 enantiomer 2 (80 mg, 0.37 mmol), 4-chloro-2-methylbenzoic acid (68 mg; 0.40 mmol), HOBt (61 mg; 0.40 mmol) and PS-DCC (310 mg of 1.3 mmol/g loading, 0.40 mmol) in DCM (4 ml) was shaken overnight. Saturated aqueous sodium bicarbonate was added and the mixture separated with a phase-sep cartridge and the organics applied directly to SCX resin. Elution with DCM, methanol and then 1M ammonia in methanol, followed by chromatography eluting with 12-100% ethyl acetate-pentane (SP4 Biotage) afforded the title product (64 mg; 43%). 1H NMR (CDCl3) δ: 0.9-1.0 (1H, m), 1.25-1.40 (1H, m), 1.4-1.6 (2H, m), 1.6-1.75 (2H, m), 1.8-1.9 (2H, m), 2.22 (6H, s), 2.41 (3H, s), 5.09 (1H, d, J=5 Hz), 7.07 (1H, d, J=5 Hz), 7.2-7.4 (8H, m). Mass Spectrum (Electrospray LC/MS): Found 371 (MH+). C22H2735ClN2O requires 370. Ret. time 2.26 min. The title product was converted to the corresponding hydrochloride salt.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07745642B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-b47023f147ae4c59b1d092eef245a220 |
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| 출처 메모 | uspto-grants-2010_06 |
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