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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491882Generated: October 30, 2026

Cyanogen Bromide → HCID 178508229, compound

https://huagongshe.com/reaction/491882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 178508038HCID 178508038—
SolventEthanolHCID 702—
ProductHCID 178508229HCID 178508229—

Reaction Steps

A solution of 4-[[4-[(5-amino-2-phenoxy-pyridin-4-ylmethyl)-amino]-4-(S)-(tetrahydro-pyran-4-yl)-butyryl]-(2-benzyloxy-ethyl)-amino]-cis-cyclohexanecarboxylic acid benzyl ester (0.5 g, 0.7 mmol) and BrCN (3M in CH2Cl2, 0.25 mL) in EtOH (20 mL) was stirred at room temperature overnight. The EtOH was evaporated. The resulting oil was stirred in diethyl ether (50 mL) for 30 min. 4-[[4-(2-Amino-6-phenoxy-4H-pyrido[3,4-d]pyrimidin-3-yl)-4-(S)-(tetrahydro-pyran-4-yl)-butyryl]-(2-benzyloxy-ethyl)-amino]-cis-cyclohexanecarboxylic acid benzyl ester was collected as a solid as its corresponding HBr salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531545B2
Source datasetuspto-grants-2009_05
ORD IDord-974faa967ce545c1aefa186647926335
Source noteuspto-grants-2009_05