Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18947045 | HCID 18947045 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 67790044 | HCID 67790044 | — |
Reaction Steps
A solution of 2.13 g (0.011 mol) of 1,3-dichloro-5,6-dihydro-4H-thieno[3,4-c]pyrrole and 2.5 ml of N,N-diisopropylethylamine in 25 ml of dimethylformamide is poured onto a mixture of 1.95 g (0.0125 mol) of 2-chloromethyl-1H-4,5-dihydroimidazole hydrochloride, 2.5 ml of N,N-diisopropylethylamine and 25 ml of dimethylformamide. The mixture is subjected to ultrasound for 8 h and is then evaporated under vacuum. The residue is dissolved in 75 ml of salt solution and extracted with 5 times 50 ml of methylene chloride. The organic solution is dried and then concentrated to produce a residue which is dissolved in 50 ml of isopropanol and treated with 14 ml of a 1N solution of hydrochloric acid in isopropanol. The crystals formed by cooling are filtered and washed with diethyl ether. 0.5 g of product is obtained. Melting point: 206°-213° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05380742 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-251f300dcc2e4407919a13926d157587 |
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| Source note | uspto-grants-1995_01 |
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