Di-tert-butyl 1-(5-cyanothiophen-2-yl)hydrazine-1,2-dicarboxylate → HCID 69090430, compound
Reaction equation
[ClH:1].N(C1C=C(C#N)SC=1)N.[C:11]([C:13]1[S:17][C:16]([N:18](C(OC(C)(C)C)=O)[NH:19]C(OC(C)(C)C)=O)=[CH:15][CH:14]=1)#[N:12]>>[Cl-:1].[C:11]([C:13]1[S:17][C:16]([NH2+:18][NH2:19])=[CH:15][CH:14]=1)#[N:12]Participants
3
Procedure
Following the same procedure as described for compound 13 (step 3, scheme 2, example 1c) except using 20 (692 mg, 2.04 mmol) instead of 12 to afford 21 (278 mg, 78%) as a brown solid. LRMS (ESI): calc. 139.0; found 140.1 (MH)+.
Sources & evidence
- ORD record
- ord-38a1cb427a69415090af08e47c5bfba8
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08338437B2
Reaction notes
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