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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830976Generated: November 1, 2026

Pyridine → HCID 22046709, compound

https://huagongshe.com/reaction/1830976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoic acid, 2-amino-5-iodo-HCID 72911—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
SolventDichloromethaneHCID 6344—
ProductHCID 22046709HCID 2204670975%

Reaction Steps

A solution of Troc-Cl (2.88 mL, 20.9 mmol) in dry dichloromethane (20 mL) was added drop wise to a solution of 5-iodoanthranilic acid 131 (5 g, 19 mmol) and pyridine (3.1 mL, 38 mmol) in dry dichloromethane (30 mL) at 0° C. The solution was stirred for 5 hours at room temperature and then washed with 1N HCl (2×25 mL), water (1×25 mL) and brine (1×25 mL). The organic phase was dried over MgSO4 and evaporated, residue was recrystallized from ethyl acetate to afford the title compound as a yellow solid (6.2 g, 75%): m.p. 248 C (ethyl acetate). 1H NMR (CDCl3, DMSO-d6) δ4.83 (s, 2H); 7.78-7.82 (dd, J=9.2, J=2.2 Hz, 1H); 8.18 (d, J=9 Hz, 1H); 8.38 (d, J=2.2 Hz, 1H); 9.0-10.5 (bs, 1H); 11.04 (s, 1H). 13C NMR (CDCl3, DMSO-d6) δ74.4, 84.6, 95.2, 117.7, 120.7, 140, 140.8, 142.8, 151.5, 169. MS: m/e (relative intensity) 437 (M−1, 60), 289 (55), 272 (37), 245 (100), 218 (27). HRMS Calculated for C10H7Cl3INO4: 436.8485. Found: 436.8485.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067511B2
Source datasetuspto-grants-2006_06
ORD IDord-e5775f0f75694b22bc69501c8904d0ea
Source noteuspto-grants-2006_06