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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857560Generated: October 30, 2026

Ethyl 2-((2-(benzo[d]thiazole-2-sulfonamido)ethyl)amino)acetate → HCID 136364038, compound

https://huagongshe.com/reaction/857560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-((2-(benzo[d]thiazole-2-sulfonamido)ethyl)amino)acetateHCID 21868443—
ReactantHCID 136364015HCID 136364015—
ProductHCID 136364038HCID 13636403868.1%

Reaction Steps

The title compound (2.48 g, 68%) was synthesized by the reaction of N-[2-(benzothiazole-2-sulfonylamino)-ethyl]-glycine ethyl ester (1.72 g, 5 mmol) and [2-N-(3,4-dimethoxybenzyloxycarbonyl)-guanin-9-yl]-acetic acid (2.02 g, 5 mmol) as per the procedure of Example 20. 1H NMR (500 MHz; DMSO-d6) δ 8.26 (dd, 1H), 8.14 (dd, 1H), 7.80 (s, 0.6H), 7.76 (s, 0.4H), 7.65 (m, 2H), 7.04 (s, 1H), 6.95 (m, 2H), 5.15 (s, 2H), 5.09 (s, 1.2H), 4.90 (s, 0.8H), 4.42 (s, 0.8H), 4.16 (q, 0.8H), 4.06 (s, 1.2H), 4.03 (q, 1.2H), 3.74 (s, 3H), 3.73 (s, 3H), 3.62 (t, 1.2H), 3.43 (t, 1.2H), 3.39 (t, 0.8H), 3.20 (t, 0.8H), 1.21 (t, 1.2H), 1.13 (t, 1.8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07145006B2
Source datasetuspto-grants-2006_12
ORD IDord-fc7c12c7c9bc493188e467f46d9f8b0b
Source noteuspto-grants-2006_12