Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505727Generated: November 1, 2026

Triethylamine → tert-butyl (NZ)-N-[[(2-methylpropan-2-yl)oxycarbonylamino]-[6-(2-phenylethyl)-5-(trifluoromethyl)-1,10-diazatricyclo[6.4.1.04,13]trideca-2,4(13),5,7-tetraen-11-yl]methylidene]carbamate

https://huagongshe.com/reaction/1505727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantN,N'-Di-Boc-thioureaHCID 5193990—
Reactant6-Phenethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydro-[1,4]diazepino[6,7,1-hi]indoleHCID 86691988—
SolventDimethylformamideHCID 6228—
Producttert-butyl (NZ)-N-[[(2-methylpropan-2-yl)oxycarbonylamino]-[6-(2-phenylethyl)-5-(trifluoromethyl)-1,10-diazatricyclo[6.4.1.04,13]trideca-2,4(13),5,7-tetraen-11-yl]methylidene]carbamateHCID 140613434—

Reaction Conditions

Temperature0 °C

Reaction Steps

Mercuric chloride (41 mg, 0.15 mmol) was added to a mixture of 6-phenethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydro-[1,4]diazepino[6,7,1-hi]indole (prepared as described in Example 2 above, 53 mg, 0.14 mmol), bis-N-Boc thiourea (38 mg, 0.14 mmol) and triethylamine (0.45 mmol) in DMF (5 mL) at 0° C. After 1 h of stirring at 0° C., ethyl acetate was added. The resulting mixture filtered and the filtrate washed sequentially with water and brine then dried (Na2SO4) and concentrated. The resulting residue was purified by reverse-phase chromatography to yield Z-tert-butyl(((tert-butoxycarbonyl)imino)(6-phenethyl-7-(trifluoromethyl)-3,4-dihydro-[1,4]diazepino[6,7,1-hi]indol-2(1H)-yl)methyl)carbamate (74 mg, MS m/z=587 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216998B2
Source datasetuspto-grants-2015_12
ORD IDord-96fee8fac3c649d58ec098b1c013790a
Source noteuspto-grants-2015_12