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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365014Generated: October 29, 2026

1,1'-Carbonyldiimidazole → Tert-butyl 1-(cyclopropylsulfonylcarbamoyl)-2-(difluoromethyl)cyclopropylcarbamate

https://huagongshe.com/reaction/1365014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantCyclopropanesulfonamideHCID 15765418—
Reactant1-(Tert-butoxycarbonylamino)-2-(difluoromethyl)cyclopropanecarboxylic acidHCID 57945043—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 1-(cyclopropylsulfonylcarbamoyl)-2-(difluoromethyl)cyclopropylcarbamateHCID 5794502584%

Reaction Steps

A mixture of 1-(tert-butoxycarbonylamino)-2-(difluoromethyl)cyclopropanecarboxylic acid (975 mg, 3.88 mmol) and CDI (755 mg, 4.66 mmol) in tetrahydrofuran (10 mL) was heated at reflux for 1 h. It was then cooled to rt and then cyclopropanesulfonamide (564 mg, 4.66 mmol) was added, followed by DBU (0.702 mL, 4.66 mmol). This mixture was stirred at rt for 18 h. It was then concentrated in vacuo, diluted with water and adjusted to pH=4 using 1 N HCl. The acidic solution was extracted with EtOAc, washed with water (5×15 mL), dried (MgSO4), and concentrated in vacuo to yield 1.6 g of the crude product as a white solid. Recrystallization from hexane/EtOAc gave 1.15 g (84%) of tert-butyl 1-(cyclopropylsulfonylcarbamoyl)-2-(difluoromethyl)cyclopropylcarbamate as a white solid. LC-MS, MS m/z 377 (M+1+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888464B2
Source datasetuspto-grants-2011_02
ORD IDord-bc329fc959004a65ba88a58edb031c23
Source noteuspto-grants-2011_02