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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349626Generated: October 30, 2026

Hydrochloric Acid → N-[2-(Benzothiazole-2-sulfonylamino)-ethyl]-N-{[6-N-(4-methoxybenzyloxycarbonyl)-adenin-9-yl]-acetyl}-glycine ethyl ester

https://huagongshe.com/reaction/349626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 21868398HCID 21868398—
ReactantEthyl 2-((2-(benzo[d]thiazole-2-sulfonamido)ethyl)amino)acetateHCID 21868443—
SolventDimethylformamideHCID 6228—
ProductN-[2-(Benzothiazole-2-sulfonylamino)-ethyl]-N-{[6-N-(4-methoxybenzyloxycarbonyl)-adenin-9-yl]-acetyl}-glycine ethyl esterHCID 21868450102.5%

Reaction Steps

To the mixture of N-[2-(benzothiazole-2-sulfonylamino)-ethyl]-glycine ethyl ester (172 mg, 0.5 mmol), [6-N-(4-methoxybenzyloxycarbonyl)-adenin-9-yl]-acetic acid (179 mg, 0.5 mmol), and HBTU (190 mg, 0.5 mmol) in DMF (2 ml) was added diisopropylethylamine (0.09 ml, 0.5 mmol) at ambient temperature. The resulting reaction mixture was stirred for 2 h at the same temperature and 1N HCl was added to the reaction mixture. The resulting precipitate product was filtered off, washed with water, and dried in vacuo to give the title compound as a white solid (0.35 g, 97%). 1H NMR (500 MHz; DMSO-d6) δ 8.97 (t, 0.6H), 8.76 (t, 0.4H), 8.64 (s, 0.4H), 8.60 (s, 0.6H), 8.53 (d, 1H), 8.28 (m, 1H), 8.17 (d, 1H), 7.66 (m, 2H), 7.40 (d, 2H), 6.95 (d, 2H), 5.41 (s, 1.2H), 5.20 (s, 0.8H), 5.18 (s, 2H), 4.46 (s, 0.8H), 4.18 (q, 0.8H), 4.08 (s, 1.2H), 4.03 (q, 1.2H), 3.75 (s, 3H), 3.70 (q, 1.2H), 3.48 (q, 1.2H), 3.42 (t, 0.8H), 3.22 (q, 0.8H), 1.24 (t, 1.2H), 1.13 (t, 1.8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179896B2
Source datasetuspto-grants-2007_02
ORD IDord-c27828a0c9f94ab99e8e50b186bb20db
Source noteuspto-grants-2007_02