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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652775Generated: October 30, 2026

Ammonia → HCID 86741588, compound

https://huagongshe.com/reaction/652775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 54119204HCID 54119204—
ReactantHCID 54502136HCID 54502136—
SolventAcetoneHCID 180—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 86741588HCID 86741588—

Reaction Steps

6.5 g of 2-methoxy-4-amino-5-methyl sulphamoyl benzoic acid, 75 ml of acetone, 14 ml of water and 3.5 ml of triethylamine (density 0.726) are placed in a 250 ml flask fitted with an agitator, a thermometer, a condenser and a dropping funnel. The solution is cooled to between 0° and +5° C. and 2.7 g of ethyl chloroformate is added drop by drop. The reaction medium is agitated for 45 minutes at room temperature then cooled to 0° C. again. 6.8 g of 1-cycloheptyl methyl-2-amino methyl pyrrolidine is added drop by drop. The medium is reacted for 2 hours then left to stand. The solvents are expelled and the solid residue dissolved in 50 ml of water and 20 ml of hydrochloric acid (density 1.18). The suspension obtained is made alkaline with ammonia. It is extracted 3 times with 50 ml of methylene chloride. The organic phase is washed twice with 50 ml of water, dried over magnesium sulphate and filtered. The filtrate is evaporated to dryness under vacuum. The residue is dissolved in 80 ml of water and 20 ml of hydrochloric acid (density 1.18). The hydrochloride crystallises. It is drained, washed with water and dried in an oven at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04673686
Source datasetuspto-grants-1987_06
ORD IDord-ce9e4f3e2d2044e7a16d701530368b17
Source noteuspto-grants-1987_06