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| (7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline] Basic information |
Product Name: | (7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline] | Synonyms: | (7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline];Ochotensimine;Spiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline], 3',4',6,8-tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylene-, (7'S)- | CAS: | 4829-36-1 | MF: | C22H23NO4 | MW: | 365.42 | EINECS: | | Product Categories: | | Mol File: | 4829-36-1.mol | |
| (7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline] Chemical Properties |
| (7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline] Usage And Synthesis |
Description | Corydalis ochotensis yields this alkaloid as an amorphous yellow-brown substance
furnishing a crystalline methiodide, m.p. 225°C (dec.); [αl 22
D + 49.2° (c 0.2,
MeOH). The ultraviolet spectrum of the free base in MeOH has two absorption
maxima at 226 and 287 mJi. When hydrogenated over Pd-C it yields a non_x0002_crystalline dihydro derivative with [α] 22
D+ 112°. The dihydromethine is,
however, crystalline, with m.p. 92°C. | References | Manske., Can. J. Res., 16B, 81 (1938) Manske., ibid, 18B, 75 (1940)McLean, Mei-Sie Lin., Tetrahedron Lett., 3819 (1964) Synthesis:
McLean, Mei-Sie Lin, Whelan., Tetrahedron Lett., 2425 (1968) Irie, Kishimoto, Uyeo., J. Chern. Soc., C, 3051 (1968) |
| (7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline] Preparation Products And Raw materials |
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