Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → 4-(3-Ethoxycarbonylpropyl)Amino-6,7,8-Trimethoxyquinazoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Chloro-6,7,8-trimethoxyquinazoline | HCID 100686 | — |
| 반응물 | 4-Aminobutyrate ethyl hydrochloride | HCID 12649661 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 4-(3-Ethoxycarbonylpropyl)Amino-6,7,8-Trimethoxyquinazoline | HCID 9798450 | 72% |
반응 단계
1.0 g of ethyl 4-aminobutyrate hydrochloride (6.0 mmol), 2 ml of triethylamine, 10 ml of tetrahydrofuran and 10 ml of 2-propanol are added to 0.50 g (2.0 mmol) of 4-chloro-6,7,8-trimethoxyquinazoline, followed by heating under reflux one whole day and night. The reaction liquid is distilled under reduced pressure to remove the solvent. The obtained residue is purified by silica gel column chromatography (ethyl acetate) and then recrystallized from ethyl acetate/hexane. Thus, 0.49 g (yield 72%) of a white crystal is obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05990117 |
| 출처 데이터셋 | uspto-grants-1999_11 |
| ORD ID | ord-f89c6bd37f1e46618a85f45d67f39c63 |
| 출처 메모 | uspto-grants-1999_11 |