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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731057Generated: November 1, 2026

Ammonium Chloride → HCID 178422617, compound

https://huagongshe.com/reaction/731057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant[4-(1,3-Dibenzyl-2-methyl-1H-indol-5-yl)-phenoxy]-acetonitrileHCID 68814248—
SolventDimethylformamideHCID 6228—
ProductHCID 178422617HCID 178422617—

Reaction Steps

The desired product was prepared using a procedure similar to step 6 of example 3. Thus, [4-(1,3-dibenzyl-2-methyl-1H-indol-5-yl)-phenoxy]-acetonitrile (0.160 g, 0.362 mmol) was reacted with NaN3 (0.118 g, 1.808 mmol) and NH4Cl (0.097 g, 1.808 mmol) in DMF (5 ml) to give the product (0.136 g, 0.280 mmol, 77%) as a white solid, mp 190-192° C. 1H NMR (DMSO-d6) δ 2.35 (s, 3H), 4.10 (s, 2H), 5.43 (s, 2H), 5.49 (s, 2H), 6.99 (d, J=7.0 Hz, 2H), 7.09-7.13 (m, 3H), 7.20-7.30 (m, 8H), 7.40 (d, J=8.4 Hz, 1H), 7.54 (d, J=8.9 Hz, 2H), 7.60 (d, J=1.7 Hz, 1H); IR (solid) 3030, 2905, 2850, 1605, 1520, 1480, 1440, 1360, 1270, and 1250 cm−1; [ESI(−)], m/z 484 (M−H)−; Anal. Calcd. for C31H27N5O: C, 76.88; H, 5.60; N, 14.42; Found: C, 76.71; H, 5.57; N, 14.37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582773B2
Source datasetuspto-grants-2009_09
ORD IDord-dfe9264dfe8e46c794c0e67ab5924326
Source noteuspto-grants-2009_09