Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 458621생성일: 2026년 10월 24일
7-Benzyl-8-chloro-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione → N-(1-(7-Benzyl-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropurin-8-yl)azepan-3-yl)-4-methylbenzenesulfonamide
https://huagongshe.com/ko/reaction/458621
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 7-Benzyl-8-chloro-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione | HCID 325372 | — |
| 반응물 | N-(Azepan-3-yl)-4-methylbenzenesulfonamide | HCID 22508595 | — |
| 용매 | 2-Methoxyethanol | HCID 8019 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | N-(1-(7-Benzyl-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropurin-8-yl)azepan-3-yl)-4-methylbenzenesulfonamide | HCID 22508573 | — |
반응 단계
7-Benzyl-8-chloro-1,3-dimethyl-3,7-dihydropurine-2,6-dione (2A) (1.03 g, 3.40 mmol) and N-(azepan-3-yl)-4-methylbenzenesulfonamide (6B) (1.00 g, 3.73 mmol) were dissolved in 2-methoxyethanol (30 ml) and triethylamine (2.4 ml), and the mixture was heated to 120° C. for 2 days. The solvents were evaporated and the crude product was dissolved in 100 ml of EtOAc and 100 ml of water. The aqueous phase was acidified with 1M potassium hydrogen sulphate until pH=2. The organic layer was separated and extracted with 50 ml of 1M aqueous potassium hydrogen sulphate, and 50 ml of brine, and dried over sodium sulphate. The solvent was evaporated and the crude product was purified by column chromatography on silica gel using EtOAc:heptane (1:1) as the eluent. Evaporation of the solvent gave compound (6C) as a white foam.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07192952B2 |
|---|
| 출처 데이터셋 | uspto-grants-2007_03 |
|---|
| ORD ID | ord-c3d53bf8551d4b14a2dee3a4e39005a7 |
|---|
| 출처 메모 | uspto-grants-2007_03 |
|---|