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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857501Generated: November 1, 2026

Pyridine → HCID 86756036, compound

https://huagongshe.com/reaction/1857501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantMethyl chloroformateHCID 6586—
ReactantHCID 86756035HCID 86756035—
SolventEthyl AcetateHCID 8857—
ProductHCID 86756036HCID 8675603687.4%

Reaction Steps

To a pre-dried flask under nitrogen atmosphere was added cis-8-amino-4-[(3,5-bis-trifluoromethyl-benzyl)-methoxycarbonyl-amino]-6-chloro-2-methyl-3,4-dihydro-2H-quinoline-1-carboxylic acid ethyl ester (Example 109) (30 mg, 0.053 mmol), followed by anhydrous dichloromethane (2 mL), pyridine (0.5 mL), and methyl chloroformate (0.016 mL, 0.21 mmol). The reaction was stirred overnight at room temperature before ethyl acetate was added, and the mixture was extracted three times with 1N HCl, followed by brine. The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to give the desired product (29 mg, 87%). MS m/z 626 (M+ +H); 1H NMR (CDCl3) δ 7.82 (bs, 1H), 7.8 (bs, 1H), 7.7 (bs, 1H), 6.68 (bs, 1H), 6.7 (bs, 1H), 3.8 (s, 3H), 3.75 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147090
Source datasetuspto-grants-2000_11
ORD IDord-664d2caca69f44c584107951a4098553
Source noteuspto-grants-2000_11