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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432189Generated: November 3, 2026

Chlorosuccinimide → HCID 22182413, compound

https://huagongshe.com/reaction/1432189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 22182417HCID 22182417—
SolventAcetic AcidHCID 176—
ProductHCID 22182413HCID 2218241371%

Reaction Steps

A mixture of t-butyl 4-(thieno[2,3-d]pyrimidin-4-ylamino)piperidine-1-carboxylate (1.00 g, 3.00 mmol) and N-chlorosuccinimide (0.39 g, 3.00 mmol) were heated in 50 mL of acetic acid for 3 h. After cooling to room temperature acetic acid was removed under reduced pressure and the remaining residue was partition in 1 M NaOH and DCM. The DCM layer was dried over Na2SO4 and evaporated under reduced pressure. The crude product was purified by silica chromatography in 5% MeOH-DCM to collect 0.78 g of product (71% yield). 1H NMR (400 MHz, CDCl3): δ 8.45 (s, 1H), 7.01 (s, 1H), 4.94 (d, 1H), 4.32 (m, 1H), 4.15 (m, 2H), 2.94 (m, 2H), 2.11 (m, 2H), 1.48 (s, 9H), 1.44 (m, 2H); MS (ESI) m/z: Calculated for C16H21ClN4O2S, 368.11; Observed: 368.8 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612078B2
Source datasetuspto-grants-2009_11
ORD IDord-e68cdbbb113e4618a033c793084dfdb4
Source noteuspto-grants-2009_11