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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079787Generated: October 31, 2026

Dichloromethane → N-Hydroxy 2-{6-[(naphthalene-2-sulfonyl)-(2-pyrrolidin-1-yl-ethyl)amino]-3-azabicyclo[3.1.0]hex-3-yl}pyrimidine-5-carboxamide

https://huagongshe.com/reaction/2079787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-(Tetrahydro-2H-pyran-2-yloxy) 2-{6-[(naphthalene-2-sulfonyl)-(2-pyrrolidin-1-ylethyl)amino]-3-azabicyclo[3.1.0]hex-3-yl}pyrimidine-5-carboxamideHCID 59367676—
SolventMethanolHCID 887—
ProductN-Hydroxy 2-{6-[(naphthalene-2-sulfonyl)-(2-pyrrolidin-1-yl-ethyl)amino]-3-azabicyclo[3.1.0]hex-3-yl}pyrimidine-5-carboxamideHCID 5936758830.2%

Reaction Steps

To N-(tetrahydro-2H-pyran-2-yloxy) 2-{6-[(naphthalene-2-sulfonyl)-(2-pyrrolidin-1-ylethyl)amino]-3-azabicyclo[3.1.0]hex-3-yl}pyrimidine-5-carboxamide (0.234 g, 0.38 mmol) was added TFA:DCM:MeOH (6 ml, 1:1:1 mixture). The mixture was stirred for 3 h at r.t. and then concentrated in vacuo. The product was purified by reverse phase HPLC to yield the title compound (60 mg, 30%). LCMS Purity >98%, m/z 523.25 [M+H]+, 1H NMR (300 MHz, d6-DMSO) δ: 1.55-1.68 (4H, m), 1.78 (1H, m), 2.25-2.34 (2H, m), 2.35-2.45 (4H, m), 2.55-2.65 (2H, m), 3.25-3.42 (5H, m), 3.54-3.63 (2H, m), 3.73-3.85 (2H, m), 7.65-7.77 (2H, m), 7.86 (1H, d, J=8.5 Hz), 8.06 (1H, d, J=7.3 Hz), 8.17 (1H, d, J=7.3 Hz), 8.24 (1H, d, J=7.3 Hz), 8.55 (1H, s), 8.61 (2H, s), 9.00 (1H, br s), 11.05 (1H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932246B2
Source datasetuspto-grants-2011_04
ORD IDord-8c0a15e72cc740f783b17bb5f74a7c15
Source noteuspto-grants-2011_04