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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176702Generated: October 30, 2026

Water → HCID 11948400, compound

https://huagongshe.com/reaction/1176702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenepropanalHCID 7707—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-(6-Methoxy-[1,5]naphthyridin-4-yl)4,5,6,7-tetrahydro-2H-indazol-5-ylamineHCID 59560648—
CatalystAcetic AcidHCID 176—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 11948400HCID 1194840036%

Reaction Steps

To a stirring solution of 2-(6-methoxy-[1,5]naphthyridin-4-yl)-4,5,6,7-tetrahydro-2H-indazol-5-ylamine (50 mg, 0.17 mmol) and 3-phenylpropionaldehyde (20 mg, 0.2 mmol) in dichloroethane (2 mL) was added NaB(OAc)3H (37 mg, 0.17 mmol) and acetic acid (2 drops). The reaction mixture was stirred overnight at RT. Water (5 mL) was added, and the aqueous layer was extracted with CH2Cl2 (3×15 mL). The combined organic layers were washed with brine (10 mL), dried (MgSO4), filtered, and concentrated. The crude material was purified on SiO2 (0-5% CH3OH/CH2Cl2) to give 24 mg (36%) of the title compound as a clear oil. MS (ESI): exact mass calculated for C25H27N5O, 413.22; m/z found, 414.5 [M+H]+. 1H NMR (400 MHz, CDCl3): 9.07 (s, 1H), 8.72-8.70 (m, 1H), 8.25-8.23 (m, 1H), 8.08-8.07 (m, 1H), 7.30-7.21 (m, 5 H), 7.18-7.16 (m, 1H), 4.09 (s, 3H), 3.06-2.90 (m, 3H), 2.80-2.68 (m, 5H), 2.46-2.40 (m, 1H), 2.19-2.16 (m, 1H), 1.93-1.86 (m, 2H), 1.77-1.67 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842810B2
Source datasetuspto-grants-2010_11
ORD IDord-879c34515c424a9dae706f93dfed5554
Source noteuspto-grants-2010_11