Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857499Generated: November 2, 2026

Water → HCID 86758100, compound

https://huagongshe.com/reaction/1857499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 13161436HCID 13161436—
ReactantHCID 131722151HCID 131722151—
SolventDichloromethaneHCID 6344—
ProductHCID 86758100HCID 8675810096.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a pre-dried flask under nitrogen atmosphere was prepared a slurry of F3CSO3NO2 (2.6 mmol) in 9 mL of dichloromethane [ref. J. Org. Chem. 1973, 38 (25), 4243]. The solution was cooled to -78° C. and a solution of cis-4-[(3,5-bis-trifluoromethyl-benzyl)-methoxycarbonyl-amino]-6-chloro-2-methyl-3,4-dihydro-2H-quinoline-1-carboxylic acid ethyl ester (Example 32) (0.72 g, 1.3 mmol) in anhydrous dichloromethane (5 mL) was added. The reaction was stirred at -78° C. for 1.5 h, then warmed to 0° C. and stirred for 1 h and 40 min. Water (30 mL) was then added, and the mixture was extracted three times with dichloromethane. The combined organic layers were dried over magnesium sulfate, filtered and concentrated in vacuo to give the title product (0.75 g, 96%). MS m/z 598 (M+ +H); 1H NMR (CDCl3) δ 7.85 (bs, 1H), 7.8 (bs, 1H), 7.7 (bs, 1H), 7.65 (bs, 1H), 7.1 (bs, 1H), 3.80 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147090
Source datasetuspto-grants-2000_11
ORD IDord-e8f41f6a583744e7aac61343ede379a9
Source noteuspto-grants-2000_11