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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36367Generated: October 24, 2026

5-Bromopentanenitrile → HCID 19438938, compound

https://huagongshe.com/en/reaction/36367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromopentanenitrileHCID 79435—
Reactant2,3-Dihydro-2-oxo-1-phenyl-3-(4-pyrimidinylmethyl)1H-indoleHCID 19438956—
ProductHCID 19438938HCID 1943893868%

Reaction Steps

By substituting 2,3-Dihydro-2-oxo-1-phenyl-3-(4-pyrimidinylmethyl)1H-indole and 5-bromopentanenitrile in Example 1, the desired product was obtained in 68% yield as an oil; NMR(CDCl3TMS): δ1.21 (m, 1H); 1.35 (m, 1H); 1.60 (m, 1H); 1.65 (m, 1H); 2.00 (m, 1H); 2.20 (m, 1H); 2.26 (m, 2H); 3.25 (d, 1H, J=14 Hz); 3.55 (d, 1H, J=14 Hz); 6.65 (d, 1H, J=8 Hz); 6.98 (m, 1H); 7.09 (m, 2H); 7.21 (m, 1H); 7.27 (m, 2H); 7.42 (m, 1H); 7.51 (t, 2H, J=7 Hz); 8.44 (d, 1H, J=5 Hz); 8.90 (s, 1H); IR(KBr): 1718, 1612, 1583, 1549, 1500, 1481, 1465, 1454, 1376, 1326, 1221, 758, 733, 700 cm-1 ; mass spec m/e 383 (M+1). HRMS: m/e calcd 383.187187, m/e found 383.185396 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05414004
Source datasetuspto-grants-1995_05
ORD IDord-139b4bd3fb3444fc96691e3bc54e13f9
Source noteuspto-grants-1995_05