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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243855Generated: October 26, 2026

1-Hydroxybenzotriazole → HCID 178451519, compound

https://huagongshe.com/reaction/243855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantTert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylateHCID 4142526—
ReactantHCID 178524291HCID 178524291—
SolventDichloromethaneHCID 6344—
ProductAmmoniaHCID 2228%
ProductHCID 178451519HCID 178451519150%

Reaction Steps

To a solution of Intermediate 15 (1.0 g, 4.73 mmol) in DCM (24 mL) was added 2-(4H-[1,2,4]triazol-3-yl)benzoic acid (895 mg, 4.73 mmol) followed by EDCl (1.36 g, 7.09 mmol), HOBt (959 mg, 7.09 mmol) and TEA (1.97 mL, 14.19 mmol). The mixture was stirred for 14 h at room temperature and then washed 2× with saturated aqueous NH4Cl solution. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. Chromatography (DCM to 8% 2M NH3 in MeOH/DCM) afforded the desired product as a pale yellow foam (1.36 g, 75%). MS (ESI): mass calculated for C20H25N5O3, 383.45, m/z found 384.1 [M+1]+. 1H NMR (500 MHz, CDCl3): 12.62 (s, 1H), 8.19-8.03 (m, 2H), 7.56-7.44 (m, 2H), 7.39-7.32 (m, 1H), 3.96-2.72 (m, 10H), 1.53-1.35 (m, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653263B2
Source datasetuspto-grants-2014_02
ORD IDord-566c314c473144c895003b18946c3393
Source noteuspto-grants-2014_02