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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785306Generated: October 31, 2026

tert-Butanol → HCID 57593699, compound

https://huagongshe.com/reaction/1785306

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57593297HCID 57593297—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Producttert-butyl N-(chlorosulfonyl)carbamateHCID 15677406—
ProductHCID 57593699HCID 5759369950.8%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Chloro[[(1,1-dimethylethoxy)carbonyl]amino]-sulfane dioxide was prepared by adding chlorosulfonyl isocyanate (32 mg, 0.23 mmol, 1.0 eq.) to a cooled solution of tert-butyl alcohol (17 mg, 0.23 mmol, 1.0eq.) and dichloromethane (2 mL) in an ice-water bath. The resulting mixture was stirred at 0-5° C. for 2-3 hr. The solution was then treated with a solution of N-(3-((4-((3-aminopropyl)amino)-5-bromo-2-pyrimidinyl)amino)phenyl)-1-pyrrolidinecarboxamide (100 mg, 0.20 mmol, 1eq.) and dichloromethane (5 mL). DMAP (20 mg, 0.16 mmol) was then added followed by the dropwise addition of DIEA (0.1 mL, 0.57 mmol). The mixture was stirred at RT for overnight. The reaction mixture was concentrated in vacuo. The residue was dissolved in TFA (2 mL), and purified by HPLC using acetonitrile/water to afford the title compound (30 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504410B2
Source datasetuspto-grants-2009_03
ORD IDord-8cc5d5ff710a4e5c8fc9fd4d32199cdd
Source noteuspto-grants-2009_03