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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351189Generated: October 30, 2026

Allyl bromide → HCID 131726277, compound

https://huagongshe.com/reaction/351189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPhosphorus tribromideHCID 24614—
ReactantDiisopropylethylamineHCID 81531—
Reactant(3R)-N-((1R)-1-((4-Chlorophenyl)methyl)-2-(4-cyclohexyl-4-(1H-1,2,4-triazol-1-ylmethyl)-1-piperidinyl)-2-oxoethyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxamideHCID 9938402—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 131726277HCID 13172627759%

Reaction Steps

resin 2 (0.65 mmol g−1 (est.), 1.49 g) in dry DCM (25 cm3) were treated with PBr3 (2.28 mmol, 216 mm3) at 20° C. for 12 h. The resin was filtered off, washed with DCM (200 cm3), dried at air and transferred to a flask with DMF (20 cm3) and THIQ (5.7 mmol, 725 mm3) was added. The resin was stirred at r.t. for 24 h, washed with DMF, MeOH, DCM, and MeOH. It was dried under high vacuum. 1.45 g (0.5 mmol g−1 (est.)) of it was resuspended in DMF (10 cm3) and allyl bromide (150 mm3, 1.7 mmol) was added. After 5 d at 20° C. the solid was filtered off, washed with DMF (100 cm3) and DCM (100 cm3). The resin was then treated with DIPEA (1.00 mmol, 175 mm3) in DCM (25 cm3). After 2 days the solid material was filtered off and washed with DCM and MeOH. Yield of resin 3 1.28 g (max. est. yield: 1.25 g). The solvent was removed from the filtrate and gave analytical pure 4 (0.47 mmol, 120 mg, 59%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183367B2
Source datasetuspto-grants-2007_02
ORD IDord-9509a590137e498dae6fd5594241a132
Source noteuspto-grants-2007_02