Formamidine acetate → 6-[(4-Chlorophenyl)-(1,2,4-triazol-1-yl)methyl]-1-methylbenzotriazole
반응식
[ClH:1].ClC1C=C[C:6]([NH:9][NH:10][CH2:11][C:12]2[CH:13]=[CH:14][C:15]3[N:19]=[N:18][N:17]([CH3:20])[C:16]=3[CH:21]=2)=CC=1.[C:22](O)(=O)[CH3:23].[CH:26](=[NH:28])N>CO>[Cl:1][C:22]1[CH:23]=[CH:16][C:21]([CH:11]([N:10]2[CH:26]=[N:28][CH:6]=[N:9]2)[C:12]2[CH:13]=[CH:14][C:15]3[N:19]=[N:18][N:17]([CH3:20])[C:16]=3[CH:21]=2)=[CH:12][CH:11]=1참가 물질
실험 절차
A mixture of 5 g of intermediate 4-a, 4.8 g of methanimidamide monoacetate and 15 ml of methanol was stirred for 1.5 hours at reflux temperature. After cooling to room temperature, the reaction mixture crystallized and there were added 30 ml of water. After stirring for 1 hour the precipitate was filtered off, washed with water and dried in vacuo at 50° C. The product was diluted with 11.8 ml of 2-propanol and the whole was treated with active charcoal for 15 min. at reflux temperature. The charcoal was filtered off while hot and washed with 2-propanol. The product was crystallized, filtered off and dried in vacuo at 50° C., yielding 3.3 g (66.0%) of (+)-6-[(4-chlorophenyl)-(1H-1,2,4-triazol-1-yl)methyl]-1-methyl-1H-benzotriazole (comp. 1-a); mp. 130°-135° C.; [α]D20 =+8.0° (conc.=10% in CH3OH); enantiomeric excess: 98.4%.
후처리
- temperatureat reflux temperature
- customthe reaction mixture crystallized
- additionthere were added 30 ml of water
- stirringAfter stirring for 1 hour the precipitate
- filtrationwas filtered off
- washwashed with water
- customdried in vacuo at 50° C
- additionThe product was diluted with 11.8 ml of 2-propanol
- additionthe whole was treated with active charcoal for 15 min.
- temperatureat reflux temperature
- filtrationThe charcoal was filtered off while hot and
- washwashed with 2-propanol
- customThe product was crystallized
- filtrationfiltered off
- customdried in vacuo at 50° C.
출처 및 근거
- ORD 기록
- ord-ec000bd974d24d0198bd8f7632827eab
- 출처 데이터셋
- uspto-grants-1997_09
- 특허 번호
- US05663354
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