HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864608Generated: October 29, 2026
Azido(trimethyl)stannane → HCID 178422701, compound
https://huagongshe.com/reaction/864608
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azido(trimethyl)stannane | HCID 5104973 | — |
| Reactant | HCID 53955749 | HCID 53955749 | — |
| Reactant | HCID 54135351 | HCID 54135351 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178422701 | HCID 178422701 | 48.9% |
Reaction Steps
A mixture of 8-[3-[N-(4-cyanocinnamoylglycyl)-N-methylamino]-2,6-dichlorobenzyloxy]-2-methylquinoline (76 mg) and trimethyltin azide (109 mg) in xylene (1 ml) was heated at 125° C. for 20 hours. After cooled, methanol-chloroform (1:4 V/V, 10 ml) and silica gel (296 mg) was added to the reaction mixture. The resulting suspension was stirred at ambient temperature for one hour. The silica gel was filtered off, and the filtrate was concentrated in vacuo. The residue was purified by preparative thin-layer chromatography eluting with methanol -chloroform (1:6) to afford 8-[2,6-dichloro-3-[N-methyl-N-[4-(5-tetrazolyl)cinnamoylglycyl]amino]benzyloxy]-2-methylquinoline (40 mg) as a pale yellow glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05563162 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-9f6973b6dd5f4b71af43b6d210160662 |
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| Source note | uspto-grants-1996_10 |
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