Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906442Generated: October 30, 2026

Triethylamine → HCID 67391050, compound

https://huagongshe.com/reaction/906442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
Reactant6-Bromo-1-oxo-1,2-dihydroisoquinoline-4-sulfonyl chlorideHCID 57439900—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67391050HCID 6739105072.8%

Reaction Steps

To a solution of tert-butyl 1,4-diazepane-1-carboxylate (0.621 g) and triethylamine (0.864 mL) in THF (12 mL) was added dropwise a solution of 6-bromo-1-oxo-1,2-dihydroisoquinoline-4-sulfonyl chloride (Example 46a, 1 g) in THF (20 mL). The reaction was stirred at room temperature for 20 min. The resulting solution was concentrated under reduced pressure, acidified with 2 M HCl, and extracted into ethyl acetate. The combined organics were dried (MgSO4), filtered and evaporated under reduced pressure to give the subtitle compound (1.097 g) that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012980B2
Source datasetuspto-grants-2011_09
ORD IDord-d40b05ca164147fabfb0fb1ea4d392dc
Source noteuspto-grants-2011_09