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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540198Generated: October 25, 2026

2,4,6-Trichloroquinazoline → N-{[3-(aminomethyl)oxetan-3-yl]methyl}-6-chloro-2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinazolin-4-amine

https://huagongshe.com/reaction/540198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrichloroquinazolineHCID 10421510—
Reactant[3-(Aminomethyl)oxetan-3-yl]methanamineHCID 10953471—
Reactant2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine 1,1-dioxideHCID 19608196—
ProductN-{[3-(aminomethyl)oxetan-3-yl]methyl}-6-chloro-2-(1,1-dioxido-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)quinazolin-4-amineHCID 71255174—

Reaction Steps

The title compound was prepared in analogy to Example 56-1 in Scheme 23 by using 2,4,6-trichloroquinazoline, oxetane-3,3-diyldimethanamine and 2,3,4,5-tetrahydro-1,4-benzothiazepine 1,1-dioxide. MS obsd. (ESI+) [(M+H)+] 474, 1H NMR (400 MHz, CD3OD) δ ppm 7.99 (d, J=6.82 Hz, 1 H), 7.94 (d, J=2.53 Hz, 1 H), 7.88 (d, J=7.07 Hz, 1 H), 7.66-7.59 (m, 1 H), 7.52-7.42 (m, 2 H), 7.42-7.36 (m, 1 H), 5.21 (brs, 2 H), 4.69-4.56 (m, 5 H), 4.51 (d, J=6.32 Hz, 2 H), 4.05 (brs, 2 H), 3.52 (t, J=5.05 Hz, 2 H), 3.04 (s, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-b9d900bf164f4515b87dc6afcec06456
Source noteuspto-grants-2014_10