Trifluoroacetic acid → HCID 178511296, compound
Reaction equation
[C:1]([C@H:3]1[CH2:6][C@H:5]([NH:7]C(=O)OC(C)(C)C)[CH2:4]1)#[N:2].[C:15]([OH:21])([C:17]([F:20])([F:19])[F:18])=[O:16]>C(Cl)Cl>[F:18][C:17]([F:20])([F:19])[C:15]([OH:21])=[O:16].[NH2:7][C@H:5]1[CH2:6][C@H:3]([C:1]#[N:2])[CH2:4]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
tert-Butyl (trans-3-cyanocyclobutyl)carbamate (0.061 g, 0.31 mmol) was stirred with TFA (2 mL) in DCM (4 mL) for 1 hour. The solvents were removed in vacuo and the residue was reconstituted in DCM and subjected to rotary evaporation an additional 2 times to rid of excess TFA in the product, which was used without further purification in Step 5.
Workup
- customThe solvents were removed in vacuo
- customsubjected to rotary evaporation an additional 2 times
- customwas used without further purification in Step 5
Sources & evidence
- ORD record
- ord-f07d0eb518f742c2895ae1c18e1f6d79
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09309246B2
Reaction notes
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