1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine → 1-Methyl-4a-phenyl-2,3,4,4a,5,6,7,8-octahydroisoquinoline
Reaction equation
CN1CCC(C2C=CC=CC=2)=CC1.[CH3:14][C:15]1[NH:16][CH2:17][CH2:18][C:19]2([C:25]3[CH:30]=[CH:29][CH:28]=[C:27](OC)[CH:26]=3)[C:24]=1[CH2:23][CH2:22][CH2:21][CH2:20]2>>[CH3:14][C:15]1[NH:16][CH2:17][CH2:18][C:19]2([C:25]3[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=3)[C:24]=1[CH2:23][CH2:22][CH2:21][CH2:20]2Participants
3
Procedure
Following the above procedure but substituting 1-methyl-4-(3-methoxyphenyl)-1,2,5,6-tetrahydropyridine for 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine, there was prepared 1-methyl-4a-(3-methoxyphenyl)-2,3,4,4a,5,6,7,8-octahydroisoquinoline. The compound distilled in the range 144°-6° C. at 0.1 torr.; yield 19.3 g.
Workup
- distillationThe compound distilled in the range 144°-6° C. at 0.1 torr
Sources & evidence
- ORD record
- ord-9c8e9ced66de4f16a228ce3510f11ffa
- Source dataset
- uspto-grants-1981_07
- Patent number
- US04277608
Reaction notes
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