Hydrochloric Acid → 2-[4-(p-Chlorbenzylamino)-6-Methyl-2-Pyrimidinylthio]Acetamidoxime
반응식
[Cl:1][C:2]1[CH:20]=[CH:19][C:5]([CH2:6][NH:7][C:8]2[CH:13]=[C:12]([CH3:14])[N:11]=[C:10]([S:15][CH2:16][C:17]#[N:18])[N:9]=2)=[CH:4][CH:3]=1.Cl.[NH2:22][OH:23].C(=O)([O-])[O-].[Na+].[Na+].Cl>CN(C)C=O.C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][NH:7][C:8]2[CH:13]=[C:12]([CH3:14])[N:11]=[C:10]([S:15][CH2:16][C:17](=[N:22][OH:23])[NH2:18])[N:9]=2)=[CH:19][CH:20]=1참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
A mixture of 10.6g. (0.035 mole) of [4-(p-chlorobenzylamino)-6-methyl-2-pyrimidinylthio]acetonitrile, 4.83 g. (0.07 mole) of hydroxylamine hydrochloride and 14.7 g. (0.14 mole) of sodium carbonate in 100 ml of N,N-dimethylformamide was heated on a steam bath for 3 hours. The mixture was filtered and the filtrate evaporated in a rotary-evaporator. The residue was triturated with petroleum ether containing a little ethyl acetate. The solid which crystallized was collected and recrystallized from ethyl acetate to give pure free base, m.p. 113°-116°. This free base was dissolved in absolute ethanol and acidified with an ethereal hydrochloric acid solution to give 3.5 g. of product, as the dihydrochloric salt, m.p. 230°-232° d.
후처리
- additionA mixture of 10.6g
- filtrationThe mixture was filtered
- customthe filtrate evaporated in a rotary-evaporator
- customThe residue was triturated with petroleum ether containing a little ethyl acetate
- customThe solid which crystallized
- customwas collected
- customrecrystallized from ethyl acetate
- customto give pure free base, m.p. 113°-116°
- customto give 3.5 g
출처 및 근거
- ORD 기록
- ord-abdb051e69f74fad84db5afa1229849c
- 출처 데이터셋
- uspto-grants-1976_04
- 특허 번호
- US03950339
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