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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529148Generated: October 30, 2026

HCID 69812225, compound → HCID 44197605, compound

https://huagongshe.com/reaction/529148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69812225HCID 69812225—
ReactantHCID 178418443HCID 178418443—
ProductHCID 44197605HCID 44197605—

Reaction Steps

(S)—N-((1-(5-Cyclopentyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)spiro[indoline-3,4′-piperidine]-4-yl)methyl)propan-2-amine was prepared as described in Example 80, substituting cyclopentylmagnesium bromide for ethylmagnesium bromide in Step 1. 1H NMR (CDCl3, 400 MHz) δ 8.62 (s, 1H), 7.08-7.26 (m, 2H), 6.97 (d, 1H), 4.01 (s, 2H), 3.88-3.97 (m, 2H), 3.42 (m, 1H), 3.14 (dd, 2H), 2.96-2.98 (m, 3H), 2.80 (dt, 2H), 2.57-2.59 (m, 1H), 2.09-2.21 (m, 3H), 1.93 (m, 1H), 1.86 (m, 2H), 1.59 (d, 1H), 1.34-1.48 (m, 6H), 1.11 (s, 6H), 0.99 (m, 1H). (S)—N-((1-(5-cyclopentyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)spiro[indoline-3,4′-piperidine]-4-yl)methyl)propan-2-amine trihydrochloride. MS (APCI+) [M+H]: 446.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346805B2
Source datasetuspto-grants-2016_05
ORD IDord-c3552fe38f2f488cad5fef9c31508b8e
Source noteuspto-grants-2016_05