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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966541Generated: October 30, 2026

Sodium Hydroxide → HCID 10158265, compound

https://huagongshe.com/reaction/966541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPyrrolidineHCID 31268—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 23393849HCID 23393849—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 10158265HCID 1015826538.3%

Reaction Steps

2-Methyl-5-(1-methyl-2-oxo-propoxy)-1H-indole-3-carboxylic acid benzyl ester (0.248 g, 0.707 mmol) and pyrrolidine (0.05 g, 0.706 mmol) were mixed together in dichloroethane and stirred under N2 at room temperature for 1 hour. The reaction was then cooled to 0° C. whereupon sodium triacetoxyborohydride (0.209 g, 0.988 mmol) was added. After 30 minutes, the reaction was then permitted to warm to rt and stirred for a further 2 hours. It was then stopped by the addition of 1N NaOH (10 mL). The mixture was then extracted with EtOAc and the combined organic layers washed with brine and dried over anhydrous Na2SO4 Purification on SiO2 (10% MeOH/CH2Cl2) gave 0.110 g (38%) of the desired compound, mp 94-98° C. 1HNMR (400 MHz, DMSO): 1.58 (d, J=6.10 Hz, 3H), 1.60 (b, 4H), 2.40 (b, 4H), 2.59 (s, 3H, ArCH3),3.35 (b, 1H), 4.43 (m, 1H), 5.26 (s, 2H), 6.69 (d, J=8.44 Hz, 1H), 7.19 (d, J=8.64 Hz, 1H), 7.28-7.44 (m, 6H), 11.72 (s, H, H). MS APCI+) m/z 407.2(MH+). Anal. Calcd for C25H30N2O3.0.20H2O: C, 3.21;H,7.47; N, 6.83. Found: C, 72.84: H, 7.57: N, 6.56 I (KBr): 3294, 2973, 1691, 1665, 1454, 1167, 1073 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951848B2
Source datasetuspto-grants-2005_10
ORD IDord-3588461edbff4056b60a01442417438c
Source noteuspto-grants-2005_10