Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540352Generated: October 26, 2026

Trifluoroacetic acid → HCID 71255289, compound

https://huagongshe.com/reaction/540352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-Boc-3-aminopyrrolidineHCID 2756370—
Reactant2,4-Dichloro-6-methylquinazolineHCID 14256483—
Reactant2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine 1,1-dioxideHCID 19608196—
Reactanttert-butyl N-(1-(aminomethyl)cyclopropyl)carbamateHCID 46864104—
ProductHCID 71255289HCID 71255289—

Reaction Steps

The title compound was prepared in analogy to Example 135-1 in Scheme 70 by using 2,4-dichloro-6-methylquinazoline, tert-butyl 3-aminopyrrolidine-1-carboxylate, 2,3,4,5-tetrahydro-1,4-benzothiazepine 1,1-dioxide and trifluoroacetic acid instead of 2,4-dichloro-6-methylquinazoline, tert-butyl [1-(aminomethyl)cyclopropyl]carbamate, 2,3,4,5-tetrahydro-1,4-benzothiazepine 1,1-dioxide and trifluoroacetic acid. MS obsd. (ESI+) [(M+H)+] 424, 1H NMR (400 MHz, DMSO-d6) δ ppm 7.92-7.82 (m, 2 H), 7.78 (br. s., 1 H), 7.69-7.56 (m, 2 H), 7.48 (t, J=7.53 Hz, 1 H), 7.34 (dd, J=8.53, 1.25 Hz, 1 H), 7.22 (d, J=6.78 Hz, 1 H), 5.08 (br. s., 2 H), 4.47 (br. s., 2 H), 3.48-2.54 (m, 7 H), 2.33 (s, 3 H), 2.25-2.00 (m, 1 H), 1.81-1.68 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-85ff82bfad89402491e4d4c20423c77f
Source noteuspto-grants-2014_10