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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540193Generated: October 26, 2026

2,4-Dichloro-6-methylquinazoline → N-{[3-(Benzylamino)oxetan-3-yl]methyl}-6-methyl-2-(1-oxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinazolin-4-amine

https://huagongshe.com/reaction/540193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6-methylquinazolineHCID 14256483—
Reactant2,3,4,5-Tetrahydrobenzo[f][1,4]thiazepine 1-oxideHCID 19608203—
Reactant3-(aminomethyl)-N-benzyloxetan-3-amineHCID 57415855—
ProductN-{[3-(Benzylamino)oxetan-3-yl]methyl}-6-methyl-2-(1-oxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinazolin-4-amineHCID 86691402—

Reaction Steps

The title compound was prepared in analogy to Example 55-1 in Scheme 23 by using 2,4-dichloro-6-methylquinazoline, 3-(aminomethyl)-N-benzyloxetan-3-amine and 2,3,4,5-tetrahydro-1,4-benzothiazepine 1-oxide. MS obsd. (ESI+) [(M+H)+] 514, 1H NMR (400 MHz, CD3OD) δ ppm 8.06 (s, 1 H), 7.81-7.77 (m, 2 H), 7.66-7.56 (m, 4 H), 7.47-7.45 (m, 2 H), 7.31-7.29 (m, 3 H), 5.45-5.35 (d, 1 H), 5.10 (brs, 1 H), 4.82-4.80 (m, 6 H), 4.71-4.69 (m, 2 H), 4.16 (s, 2 H), 3.51 (m, 2 H), 2.46 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-c45fc820a5b04cd88737c8551f417cc5
Source noteuspto-grants-2014_10