Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929234Generated: November 1, 2026

Triethylamine → HCID 131735106, compound

https://huagongshe.com/reaction/929234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 131735104HCID 131735104—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 131735106HCID 131735106—

Reaction Steps

Triethylamine (91 uL, 0.653 mmol) was added to a ice cold mixture of [(3R,3aR,6R,6aS)-3-[1-allyl-6-chloro-5-(5,6-dihydro-4H-pyrrolo[3,4-c]pyrazol-2-yl)imidazo[4,5-b]pyridin-2-yl]oxy-2,3,3a,5,6,6a-hexahydrofuro-[3,2-b]furan-6-yl]oxy-tert-butyl-dimethyl-silane 2,2,2-trifluoroacetic acid (86.4 mg, 0.128 mmol) and methane sulfonyl chloride (16 uL, 0.205 mmol) in DCM (1.0 ml). After 20 minutes, the reaction mixture was diluted with EtOAc (30 ml), water (20 ml) and 2N HCl (2 mL). The EtOAc layer was washed with brine (10 mL), dried over MgSO4, filtered, and evaporated under reduced pressure to give an oil. The oil was purified on preparative silica plates (2×1000 u developed with 1:1 EtOAc/hexanes) to give the title compound. LC-MS: calculated for C27H37ClN6O6SSi 636.20 observed m/e: 637.13 (M+H)+ (Rt 1.35/2 min)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290517B2
Source datasetuspto-grants-2016_03
ORD IDord-6519766d814e4ea0ab0a3bf64969b0f0
Source noteuspto-grants-2016_03