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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402811Generated: October 29, 2026

Formic Acid → HCID 59536838, compound

https://huagongshe.com/reaction/2402811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantPyridineHCID 1049—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 59536913HCID 59536913—
SolventDichloromethaneHCID 6344—
ProductHCID 59536838HCID 59536838—

Reaction Conditions

Temperature0 °C

Reaction Steps

A quantity of 171 μl (1.97 mmol) of chlorosulphonyl isocyanate was admixed under argon at 0° C., with vigorous stirring, with 74 μl (1.97 mmol) of anhydrous formic acid. Following the addition, the reaction mixture solidified within seconds. A quantity of 2 ml of dichloromethane was added. The reaction mixture was then stirred further at 0° C. for 1 h and then RT for 8 h. Thereafter it was cooled to 0° C. again and admixed with a solution of 400 mg (1.31 mmol) of the compound from Example 59A and 159 μl (1.97 mmol) of pyridine in 2 ml of dichloromethane. The cooling bath was removed and the reaction mixture was stirred overnight at RT. For work-up, 5 ml of water and 5 ml of ethyl acetate were added. After 10 min, the mixture was diluted with 100 ml of ethyl acetate, and washed twice with water and once with saturated aqueous sodium chloride solution. The organic phase was dried over sodium sulphate and freed from the solvent on a rotary evaporator. The residue was purified by preparative HPLC [Method 10]. The product fraction was freed from the solvent on a rotary evaporator. Drying in an HV gave 260 mg (52% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796324B2
Source datasetuspto-grants-2014_08
ORD IDord-9490e093c8d74177b004059337edaa02
Source noteuspto-grants-2014_08