Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251079Generated: November 1, 2026

Ammonium Chloride → HCID 69217202, compound

https://huagongshe.com/reaction/2251079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 24990692HCID 24990692—
SolventEthanolHCID 702—
ProductHCID 69217202HCID 69217202—

Reaction Steps

To a solution of (S)-(2-chloro-phenyl)-[7-(2,6-difluoro-phenyl)-2-(2-hydroxy-1,2-dimethyl-propylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-methanone, 8, (1.0 g, 2.1 mmol) in ethanol (2.4 mL) is added sodium borohydride (0.3 g, 8.5 mmol) and the mixture stirred overnight at room temperature. Aqueous ammonium chloride solution is then added and the mixture is extracted with EtOAc several times and the organic phases combined washed with water, brine, dried (MgSO4), filtered and concentrated in vacuo. The resulting residue is purified over silica (50% EtOAc/hexanes, then 100% EtOAc) to afford 470 mg of the desired product as a yellow solid: 1H NMR (300 MHz, CDCl3) δ 8.37 (s, 1H), 7.44-7.36 (m, 2H), 7.22-7.17 (m, 3H), 7.08 (t, J=8.8 Hz, 2H), 6.95 (dd, J=8.4, 8.0 Hz, 1H), 6.32 (d, J=13.2 Hz, 1H), 6.00 (s, 1H), 3.81 (m, 1H), 1.12-1.08 (m, 9H); HRMS calcd for C24H23ClF2N4O2 (M+H)+ 473.1556, found 473.1542.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319102B1
Source datasetuspto-grants-2008_01
ORD IDord-2c86c3eadc7540e0b0b291f6609e6cb0
Source noteuspto-grants-2008_01