Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655560Generated: November 2, 2026

Chlorotrimethylsilane → HCID 59149921, compound

https://huagongshe.com/reaction/655560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant3,4-Dichlorophenyl isocyanateHCID 7607—
ReactantTriethylamineHCID 8471—
ReactantHCID 67080751HCID 67080751—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59149921HCID 5914992162%

Reaction Steps

A solution of 0.066 g (0.21 mmol) of 4-[(S)-3-((S)-4-hydroxy-6-aza-spiro[2.5]oct-6-yl)-1-hydroxymethyl-propyl]-[1,4]diazepan-5-one (example 51B) 1.3 ml of N,N-dimethylformamide was treated at room temperature with 0.097 ml (0.70 mmol) of triethylamine and 0.088 ml (0.70 mmol) of chlorotrimethylsilane. The suspension was diluted with 1 ml of dichloromethane and stirred over night at room temperature. A solution of 0.044 g (0.23 mmol) of 3,4-dichlorophenyl isocyanate was added and stirred for 3 h at room temperature. The reaction was evaporated under reduced pressure, redissolved in 2 ml of methanol and 0.2 ml of 1 M aq. hydrochloric acid solution and after 5 min again evaporated. Partitioning between sat. aq. sodium hydrogencarbonate solution and dichloromethane (3×), drying of the organic phase over Na2SO4 and purification by flash silica gel column (dichloromethane/methanol 95:5 to 4:1) yielded 0.065 g (61%) of the title compound as yellow foam. MS: 499.2 (MH+, 2Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071586B2
Source datasetuspto-grants-2011_12
ORD IDord-0c053280e70b485aa18c9603d1aaa96c
Source noteuspto-grants-2011_12