Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540192Generated: October 26, 2026

2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepine 1-oxide → N-[(3-Aminooxetan-3-yl)methyl]-6-methyl-2-(1-oxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinazolin-4-amine

https://huagongshe.com/reaction/540192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepine 1-oxideHCID 19608203—
ReactantN-(3-Aminooxetan-3-ylmethyl)-2-chloro-6-methylquinazolin-4-amineHCID 86691401—
Solvent1-ButanolHCID 263—
ProductN-[(3-Aminooxetan-3-yl)methyl]-6-methyl-2-(1-oxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinazolin-4-amineHCID 71262235—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of N-(3-aminooxetan-3-ylmethyl)-2-chloro-6-methylquinazolin-4-amine (140 mg, 0.5 mmol) and 2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide (270 mg, 1.5 mmol) in n-butanol (10 mL) was heated at 160° C. for 30 minutes. After the resulting mixture was concentrated in vacuo, the residue was purified by preparative HPLC to afford the pure product as a solid. MS obsd. (ESI+) [(M+H)+] 424, 1H NMR (400 MHz, CD3OD) δ ppm 8.01 (s, 1 H), 7.83-7.79 (m, 2 H), 7.66-7.52 (m, 4 H), 5.45-5.41 (d, 1 H), 5.10 (brs, 1 H), 4.80-4.72 (m, 6 H), 4.39 (s, 2 H), 3.51 (s, 2 H), 2.45 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-e4c1b56289064299a38d1004fb7dca41
Source noteuspto-grants-2014_10