Acetone → (5R,7R)-4-(1'-benzyl-4-((isopropylamino)methyl)spiro[indoline-3,4'-piperidine]-1-yl)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-yl 4-nitrobenzoate

Participants

Role	Name	HCID	Charge
Reactant	Acetone	HCID 180	—
Reactant	(5R,7R)-4-(4-(aminomethyl)-1'-benzylspiro[indoline-3,4'-piperidine]-1-yl)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-yl 4-nitrobenzoate trihydrochloride	HCID 69812752	—
Product	(5R,7R)-4-(1'-benzyl-4-((isopropylamino)methyl)spiro[indoline-3,4'-piperidine]-1-yl)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-yl 4-nitrobenzoate	HCID 68760584	—

Reaction Steps

(5R,7R)-4-(1′-benzyl-4-((isopropylamino)methyl)spiro[indoline-3,4′-piperidine]-1-yl)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-yl 4-nitrobenzoate was prepared by the procedures described in Example 18, substituting (5R,7R)-4-(5-chlorospiro[indoline-3,4′-piperidine]-1-yl)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-01 dihydrochloride with (5R,7R)-4-(4-(aminomethyl)-1′-benzylspiro[indoline-3,4′-piperidine]-1-yl)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-yl 4-nitrobenzoate trihydrochloride, and substituting formaldehyde with acetone. LCMS (APCI+) m/z 647 [M+H]+; Rt=3.32 min.

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US09346805B2
Source dataset	uspto-grants-2016_05
ORD ID	ord-dbcaa819211b43e9be1d732139d93834
Source note	uspto-grants-2016_05