Ammonia → 2-Chloroadenosine
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Cl[C:2]1(O)[NH:19][C:18](N)=[N:17][C:16]2[N:6]([C@@H:7]3[O:15][C@H:12]([CH2:13][OH:14])[C@@H:10]([OH:11])[C@H:8]3[OH:9])[CH:5]=[N:4][C:3]1=2.C([C@@]1(O)[C@](C(=O)C)(O)[C@@H](C(C(=O)C)O)O[C@H]1N1C2N=C(N)NC(Cl)(O)C=2N=C1)(=O)C.N([O-])=O.[Na+].[ClH:56].[NH3:57]>>[Cl:56][C:18]1[N:19]=[C:2]([NH2:57])[C:3]2[N:4]=[CH:5][N:6]([C:16]=2[N:17]=1)[C@@H:7]1[O:15][C@H:12]([CH2:13][OH:14])[C@@H:10]([OH:11])[C@H:8]1[OH:9]참가 물질
실험 절차
The starting material, 2-chloroadenosine of the formula (II) used in the above Process 1 can be obtained in high yield from 6-chloroguanosine or a 2',3',5'-triacyl-6-chloroguanosine as disclosed in Japanese Patent Application OPI No. 48,496/1973. That is, 6-chloroguanosine or a 2',3',5'-triacyl-6-chloroguanosine, e.g., 2',3',5'-triacetyl-6-chloroguanosine, is first reacted with sodium nitrite and hydrochloric acid in ice-water and thereafter the reaction mixture is neutralized with, for example, aqueous ammonia. The resulting reaction mixture is then extracted with a solvent such as methylene chloride and the extract containing 2,6-dichloropurine riboside is treated without isolation of the riboside, with a methanolic solution saturated with anhydrous ammonia gas and the mixture is allowed to react at a temperature of about 100°C for about 5 hours in a sealed tube to obtain the desired 2-chloroadenosine of the formula (II) in about 60% yield. The preparation of the starting material of the formula (II) will be hereinafter described in greater detail in Reference Example 1.
후처리
- customThe resulting reaction mixture
- extractionis then extracted with a solvent such as methylene chloride
- additionthe extract containing 2,6-dichloropurine riboside
- additionis treated without isolation of the riboside, with a methanolic solution saturated with anhydrous ammonia gas
- customto react at a temperature of about 100°C for about 5 hours in a sealed tube
출처 및 근거
- ORD 기록
- ord-1de93a8748ad41deafc61b65e1d9201f
- 출처 데이터셋
- uspto-grants-1976_07
- 특허 번호
- US03968102
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