Synthese eines neuen Thienospirans: 6,7-Dihydro-1′-methyl-spiro[benzo[b]thiophen-4(5H),2′-piperidin]
✍ Scribed by Dipl.-Ing. Dr. Hannes Fröhlich; Dipl.-Ing. Günter Gmeiner; Prof. Dr. Fritz Sauter
- Book ID
- 105353781
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 524 KB
- Volume
- 332
- Category
- Article
- ISSN
- 1615-4150
No coin nor oath required. For personal study only.
✦ Synopsis
Synthesis of a New Thienospiran: 6,7‐Dihylro‐1′‐methyl‐spiro[benzo[j]thioxhen‐4(5H),2′‐piperidine]
The title spiro compound 6 – a N‐methyl derivative of a new parent system ‐ has been synthesized from nitrile 8 via 4‐phenoxybutylation, followed by modified Schmidt degradation, ensuing O‐deprotection and final cyclization. The constitution of the target compound and of all intermediates is established by ^1^H‐n.m.r. and ^13^C‐n.m.r.‐spectroscopy and by microelementary analysis.
📜 SIMILAR VOLUMES
## Abstract magnified image Reactions of 3‐chlorobenzo[__b__]thiophene‐2‐carbonyl chloride with 2‐alkyl‐2‐aminopropanamides have been used to prepare a series of carboxamides **1a‐d** (yields 61‐85%). The products were submitted to base‐catalysed ring closure reactions to give the corresponding 4,
## Abstract Several syntheses of 4,5‐dihydro‐10 __H__‐benzo[5,6]‐cyclohepta[1, 2‐__b__]thiophen‐10‐one (I b) are described. The pharmacological properties of the compounds XIII, which derive from IB through basic substitution on position 10, are briefly mentioned.
## 3-(3-Methoxybenzoyl 6,6-trimethyl-4,5,6,7-tetrahydrospiro[benzo[b] furan-2(3H),3 0 0 0 (2 0 0 0 H)-1H-indole]-4,2 0 0 0 -dione