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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N,N'-Di-Boc-thiourea | HCID 5193990 | — |
| Reactant | 6-Phenethyl-7-(trifluoromethyl)-1,2,3,4-tetrahydro-[1,4]diazepino[6,7,1-hi]indole | HCID 86691988 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 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 | HCID 140613434 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216998B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-96fee8fac3c649d58ec098b1c013790a |
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| Source note | uspto-grants-2015_12 |
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