HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276201Generated: October 30, 2026
HCID 22115821, compound → HCID 178480075, compound
https://huagongshe.com/reaction/1276201
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22115821 | HCID 22115821 | — |
| Reactant | Ethyl thiophene-2-carboximidothioate--hydrogen chloride (1/1) | HCID 70131116 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178480075 | HCID 178480075 | — |
Reaction Steps
2-Methyl-1,2,3,4-tetrahydroisoquinolin-7-ylamine hydrochloride (34.66 g) in 95% ethanol (600 ml) was warmed to 65° C. to dissolve most of the solids, and the mixture was then allowed to cool with stirring. The next day, the fine suspension of solids was treated with 2-thiophenecarboximidothioic acid, ethyl ester, hydrochloride (41 g) and stirred at 23° C. All solids had dissolved by 2 h, and by 4 h new solids had precipitated. The mixture was treated with concentrated hydrochloric acid (2 ml). The mixture was cooled to 0° C. and stirred for 30 minutes. The solids were filtered off, washed with ethanol (2×50 ml), and air dried to provide N-(2-methyl-1,2,3,4-tetrahydroisoquinolin-7-yl)-2-thiophenecarboximidamide dihydrochloride, m.p. 142-146° C.; MS m /z 272 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06166030 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-c085f190d14d4c0c8018d27c2595d44e |
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| Source note | uspto-grants-2000_12 |
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