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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222690Generated: October 30, 2026

Ethyl 2-((2-(benzo[d]thiazole-2-sulfonamido)ethyl)amino)acetate → HCID 21868395, compound

https://huagongshe.com/reaction/2222690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-((2-(benzo[d]thiazole-2-sulfonamido)ethyl)amino)acetateHCID 21868443—
ReactantHCID 21868451HCID 21868451—
ProductHCID 21868395HCID 2186839597.6%

Reaction Steps

The title compound (6.28 g, 96%) was synthesized by the reaction of N-[2-(benzothiazole-2-sulfonylamino)-ethyl]-glycine ethyl ester (3.26 g, 9.5 mmol) and [6-N-(3,4-dimethoxybenzyloxycarbonyl)-adenin-9-yl]-acetic acid (3.50 g, 9.03 mmol) as per the procedure of Example 27. 1H NMR (500 MHz; DMSO-d6) δ 10.58 (s, 1H), 8.98 (brs, 0.6H), 8.77 (brs, 0.4H), 8.57 (s, 0.4H), 8.53 (s, 0.6H), 8.29 (d, 1H), 8.27 (m, 1H), 8.17 (d, 1H), 7.65 (m, 2H), 7.08 (s, 1H), 6.98 (d, 1H), 6.94 (d, 1H), 5.35 (s, 1.2H), 5.15 (s, 0.8H), 5.12 (s, 2H), 4.45 (s, 0.8H), 4.18 (q, 0.8H), 4.07 (s, 1.2H), 4.01 (q, 1.2H), 3.75 (s, 3H), 3.74 (s, 3H), 3.70 (t, 1.2H), 3.48 (t, 1.2H), 3.42 (t, 0.8H), 3.22 (t, 0.8H), 1.23 (t, 1.2H), 1.12 (t, 1.8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371859B2
Source datasetuspto-grants-2008_05
ORD IDord-6e3bccf3112b454c927a8f8bb02710fd
Source noteuspto-grants-2008_05