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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470299Generated: October 31, 2026

Triethylamine → HCID 45141621, compound

https://huagongshe.com/reaction/1470299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
ReactantHCID 45139442HCID 45139442—
Solvent1-ButanolHCID 263—
ProductHCID 45141621HCID 4514162169%

Reaction Conditions

Temperature100 °C

Reaction Steps

A degassed mixture of crude N-(4-amino-piperidin-4-ylmethyl)-4-chloro-benzamide dihydrochloride (6.1 mg), 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (2.6 mg, 0.016 mmol), triethylamine (16 μL, 0.09 mmol) and n-butanol (0.3 mL) was stirred at 100° C. for 17 hours. The solvents were concentrated. The crude mixture was first purified on an SCX-II acidic resin, eluting with methanol then 2M ammonia-methanol, and then by preparative TLC, eluting with 15% methanol-dichloromethane, to give N-[4-amino-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-piperidin-4-ylmethyl]-4-chloro-benzamide (3.3 mg, 0.009 mmol, 69% over 2 steps). LC-MS (LCT2) m/z 385 [M+H+], Rt 2.58 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006430B2
Source datasetuspto-grants-2015_04
ORD IDord-648e8e10d6114820aac7b06dea0d5f3c
Source noteuspto-grants-2015_04