Phosphorus oxychloride → HCID 70530187, 화합물
반응식
[C:1]([NH:4][CH2:5][C:6]1[C:11]([CH2:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:10][CH:9]=[CH:8][N:7]=1)(=[O:3])[CH3:2].P(Cl)(Cl)([Cl:22])=O>>[OH2:3].[ClH:22].[CH3:2][C:1]1[N:7]2[CH:8]=[CH:9][CH:10]=[C:11]([CH2:12][CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[C:6]2=[CH:5][N:4]=1.[CH3:2][C:1]1[N:7]2[CH:8]=[CH:9][CH:10]=[C:11]([CH2:12][CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[C:6]2=[CH:5][N:4]=1.[ClH:22]참가 물질
실험 절차
Heat a solution of 3.1 gm of the product of Example 8 and 40 ml phosphorous oxychloride at 100° for 20 minutes. Cool to room temperature and remove the phosphorous oxychloride under reduced pressure. Partition the residue between chloroform and an aqueous solution of sodium bicarbonate. Separate the chloroform layer, wash it with brine and dry over potassium carbonate. Filter the dry solution and remove the chloroform under reduced pressure. Dissolve the residue in absolute ethanol and add an ethanolic solution of hydrogen chloride. Remove the ethanol under reduced pressure. Triturate the resulting residue in ether to obtain 3-methyl-8-(2-phenylethyl)imidazo[1,5-a]pyridine hydrochloride hemihydrate as an amorphous, hygroscopic solid.
후처리
- customremove the phosphorous oxychloride under reduced pressure
- customPartition the residue between chloroform
- customSeparate the chloroform layer
- washwash it with brine
- dry with materialdry over potassium carbonate
- filtrationFilter the dry solution
- customremove the chloroform under reduced pressure
- dissolutionDissolve the residue in absolute ethanol
- additionadd an ethanolic solution of hydrogen chloride
- customRemove the ethanol under reduced pressure
- customTriturate the resulting residue in ether
출처 및 근거
- ORD 기록
- ord-2e8fb9f195424d87adba6f59c6c577a7
- 출처 데이터셋
- uspto-grants-1983_10
- 특허 번호
- US04409226
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