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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161865Generated: October 29, 2026

Trifluoroacetic acid → HCID 24965796, compound

https://huagongshe.com/reaction/1161865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantHCID 59519096HCID 59519096—
ProductHCID 24965796HCID 2496579668%

Reaction Steps

4-[3-(tert-Butylcarbamoylmethyl)-2-(3-chlorophenyl)-4-oxo-3,4-dihydroquinazolin-6-yl]perhydro-1,4-diazepine-1-carboxylic acid tert-butyl ester (INTERMEDIATE VIII.1) (38.9 mg, 0.068 mmol) was treated with TFA:DCM (1:1 (v/v), 1 mL) and the solution stirred at room temperature for 40 min. The volatiles were removed in vacuo and the residue partitioned between DCM and 1 M NaOH (aq.). The organics were dried (Na2SO4) and concentrated in vacuo to yield N-tert-butyl-2-[2-(3-chlorophenyl)-4-oxo-6-perhydro-1,4-diazepin-1-yl-4H-quinazolin-3-yl]acetamide (EXAMPLE 1a) (27 mg, 0.046 mmol, 68%) as the trifluoroacetic acid salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820649B2
Source datasetuspto-grants-2010_10
ORD IDord-9d10390594104ace8842eb30fe7e8043
Source noteuspto-grants-2010_10