HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 54312022, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | ethyl 2-amino-6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate | HCID 207319 | — |
| Solvent | Ethyl orthoformate | HCID 31214 | — |
| Product | HCID 54312022 | HCID 54312022 | 97% |
Reaction Steps
3.2 ml of acetic anhydride were added to 40.0 g (167 mmol) of 5 2-amino-3-carboethoxy-6-methyl-4,5,6,7-tetrahydrothieno-[2,3-c]pyridine in 250 ml of triethyl orthoformate and the mixture was boiled under nitrogen and at reflux for 3 h. After that, the mixture was evaporated right down at 80° C. on a rotary evaporator. 48.0 g (97%) of crude product were isolated as a dark oil, which is sufficiently pure for further reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06387912B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-c9ed9e74f02f4561a006b721d6a72a68 |
| Source note | uspto-grants-2002_05 |