HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910451Generated: October 31, 2026
2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine 1,1-dioxide → HCID 71548636, compound
https://huagongshe.com/reaction/1910451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine 1,1-dioxide | HCID 19608196 | — |
| Reactant | HCID 86680733 | HCID 86680733 | — |
| Reactant | HCID 86680734 | HCID 86680734 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 71548636 | HCID 71548636 | — |
| Product | HCID 71548637 | HCID 71548637 | — |
Reaction Steps
A mixture of N-[(3-aminooxetan-3-yl)methyl]-2-chlorothieno[3,2-d]pyrimidin-4-amine and N-[3-(aminomethyl)oxetan-3-yl]-2-chlorothieno[3,2-d]pyrimidin-4-amine (184 mg, 0.66 mmol), 6,7,8,9-tetrahydro-5-thia-8-aza-benzocycloheptene-5,5-dioxide (680 mg, 3.44 mmol) in n-Butanol (1 mL) was heated at 160° C. for 30 min. The crude was purified by preparative HPLC to afford N-[(3-aminooxetan-3-yl)methyl]-2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)thieno[3,2-d]pyrimidin-4-amine and N-[3-(aminomethyl)oxetan-3-yl]-2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)thieno[3,2-d]pyrimidin-4-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08604019B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-2307a7509920415eb715ecaf5c44e53f |
|---|
| Source note | uspto-grants-2013_12 |
|---|