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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine 1,1-dioxideHCID 19608196—
ReactantHCID 86680733HCID 86680733—
ReactantHCID 86680734HCID 86680734—
Solvent1-ButanolHCID 263—
ProductHCID 71548636HCID 71548636—
ProductHCID 71548637HCID 71548637—

Reaction Conditions

Temperature160 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604019B2
Source datasetuspto-grants-2013_12
ORD IDord-2307a7509920415eb715ecaf5c44e53f
Source noteuspto-grants-2013_12