반응식
[CH:1]([NH2:4])([CH3:3])[CH3:2].C([N:7]([CH2:10]C)[CH2:8][CH3:9])C.C1(C2[N:20]=[C:19]([Cl:21])[N:18]=[C:17](Cl)[N:16]=2)CC1.[CH3:23]C(C)=O>>[Cl:21][C:19]1[N:18]=[C:17]([NH:4][CH:1]2[CH2:3][CH2:2]2)[N:16]=[C:10]([NH:7][CH:8]([CH3:23])[CH3:9])[N:20]=1참가 물질
5
실험 절차
A mixture of 9.5 g of isopropylamine and 16.2 g of triethylamine was added drop-by-drop to a stirred solution of 33 g of 9A in 500 ml of dry acetone at room temperature. The reaction was monitored by thin layer chromatography and further isopropylamine was added until only one product was shown. The solvent was evaporated, and the residue was treated with a 1:1 v:v mixture of ice water and ether. The ether phase was separated and dried (MgSO4), and the solvent was evaporated to give 2-chloro-4-(cyclopropylamino)-6-(1-methylethylamino)-1,3,5-triazine (9B), as a white solid, m.p.: 160.5°-161° C.
후처리
- additionwas added until only one product
- customThe solvent was evaporated
- additionthe residue was treated with a 1:1 v
- additionv mixture of ice water and ether
- customThe ether phase was separated
- dry with materialdried (MgSO4)
- customthe solvent was evaporated
출처 및 근거
- ORD 기록
- ord-2d7bbb286e8c41f193233fc80a915127
- 출처 데이터셋
- uspto-grants-1985_07
- 특허 번호
- US04528027
연결된 노트
불러오는 중…