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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079820Generated: October 31, 2026

TFA DCM MeOH → N-Hydroxy 2-[5-(naphthalene-2-sulfonyl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl]pyrimidine-5-carboxamide

https://huagongshe.com/reaction/2079820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTFA DCM MeOHHCID 19108260—
ReactantN-(1-isobutoxyethoxy) 2-[5-(naphthalene-2-sulfonyl)-hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl]-pyrimidine-5-carboxamideHCID 59367582—
ProductN-Hydroxy 2-[5-(naphthalene-2-sulfonyl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl]pyrimidine-5-carboxamideHCID 5936764450%

Reaction Steps

To N-(1-isobutoxyethoxy) 2-[5-(naphthalene-2-sulfonyl)-hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl]-pyrimidine-5-carboxamide (0.255 g, 0.5 mmol) was added TFA/DCM/MeOH (5 ml, 1:2:2 mixture). The solution was stirred for 2 h, then concentrated under vacuum. The residue was purified by reverse phase HPLC to yield the desired product (95 mg, 50%). LCMS purity >98%, m/z 440 [M+H]+, 1H NMR (300 MHz, d6-DMSO) δ: 2.90 (2H, br s), 3.24 (4H, dd, J=3.3, 10 Hz), 3.45 (2H, dd, J=6.8, 9.8 Hz), 3.61 (2H, dd, J=6.7, 11.4 Hz), 7.62-7.77 (2H, m), 7.83 (1H, dd, J=1.1, 8.5 Hz), 8.06 (1H, d, J=7.8 Hz), 8.13 (1H, d, J=8.8 Hz), 8.17 (1H, d, J=8.2 Hz), 8.47 (1H, s), 8.55 (2H, s), 11.02 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932246B2
Source datasetuspto-grants-2011_04
ORD IDord-b6a6a9ce98fa4241b9784809ccc26768
Source noteuspto-grants-2011_04